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Maryland FDA Recalls — Food, Drug, and Medical Device (Past 90 Days)

Source: U.S. Food and Drug Administration (FDA) · openFDA Enforcement API · trailing 90-day window
65
Total active
25
Food
20
Drug
20
Medical Device
What "class" means

The FDA assigns every recall one of three classes based on the severity of harm if a person uses the product:

Class I
Reasonable probability of serious adverse health consequences or death. Stop using immediately and follow return instructions.
Class II
Use may cause temporary or medically reversible adverse effects. Probability of serious harm is remote.
Class III
Not likely to cause adverse health effects — usually quality, labeling, or minor purity issues.

🥗 Food Recalls

25 active in the past 90 days · FDA Food & Cosmetic Enforcement
Jul 2, 2026
H-1181-2026
Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 1
Recalled by Frutas y Hortalizas del Sur S.A.
Potential E. coli O145:H28 Contamination
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
H-1149-2026
Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1
Recalled by Fresh & Ready Foods LLC
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chic
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
H-1148-2026
Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is
Recalled by Fresh & Ready Foods LLC
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw b
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 23, 2026
H-1143-2026
Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough, 8-oz pouch 12 cookies per po
Recalled by Bear Stewart Co
undeclared soy
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 23, 2026
H-1144-2026
Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged
Recalled by Trafa Pharmaceutical Inc.
Potential contamination with Salmonella
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 23, 2026
H-1150-2026
High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contai
Recalled by Lehi Valley Trading Company, Inc
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packag
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 21, 2026
H-1174-2026
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place so
Recalled by AMY'S KITCHEN INC.
Potential for spoilage.
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 18, 2026
H-1175-2026
OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yu
Recalled by Fayus Inc.
Undeclared peanuts
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 18, 2026
H-1154-2026
Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48
Recalled by General Mills James Ford Bell Technical Center
Potential foreign material (glass)
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 18, 2026
H-1155-2026
Pillsbury Bread Rolls, Kaiser Roll Dough. 144 units / 2.5oz each. Net Wt. 22.5 lb (10.2k
Recalled by General Mills James Ford Bell Technical Center
Potential foreign material (glass)
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 17, 2026
H-1129-2026
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 o
Recalled by MARS SNACKING
Potential contamination with plastic material
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 17, 2026
H-1135-2026
Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Visi
Recalled by Provision Health Corp. dba PH Labs
Dietary supplement product Vista MAX contains undeclared Yellow#5.
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 17, 2026
H-1134-2026
Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Se
Recalled by Provision Health Corp. dba PH Labs
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 17, 2026
H-1130-2026
MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Protein Vegan Sausage Patties, N
Recalled by MARS SNACKING
Potential contamination with plastic material
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 14, 2026
H-1125-2026
FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DA
Recalled by Western Mixers Produce & Nuts, Inc.
Undeclared peanuts.
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 12, 2026
H-1137-2026
a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0
Recalled by NARA ORGANICS INC
Product may be contaminated with Clostridium botulinum.
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
H-1147-2026
Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual marshmallows packaged
Recalled by Wondermade LLC
Foreign material: small metal pieces
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 9, 2026
H-1136-2026
Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 60
Recalled by Fry Pie Factory LLC
Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 9, 2026
H-1151-2026
Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH
Recalled by Wells Enterprises, Inc.
Elevated coliforms
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 8, 2026
H-0950-2026
Al Yaman Halawa Extra Pistachio 907g (31.994 oz) plastic jars, UPC 5 287000 098083, 12 ret
Recalled by GREENWORLD FOOD EXPRESS (USA) LLC
Product may be contaminated with Salmonella
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 4, 2026
N/A
Le Chef Bakery branded Mini Italian Pastry Assortment; 2.5 lbs/cs; (40 pieces/cs); package
Recalled by Le Chef Bakery
undeclared colors (yellow#5)
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 3, 2026
H-1157-2026
WY Duck Sauce, 0.35 oz. (10 g), flexible film packets, 500 packets per case.
Recalled by W.Y. Industries, Inc.
Product may contain metal fragments.
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 2, 2026
H-0938-2026
MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein,
Recalled by Mothers' Milk Bank of Louisiana at Ochsner Baptist
Potential physical contamination: dark spot was noticed on the bottom of container.
CLASS III Voluntary: Firm initiated
FDA record ↗
Jun 1, 2026
H-1080-2026
Dried Herring Fish 7 oz.
Recalled by Prime Food Processing LLC.
Improperly eviscerated which may result in Clostridium botulinum contamination
CLASS I Voluntary: Firm initiated
FDA record ↗
May 28, 2026
H-1095-2026
Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.43 oz. (1 lb. 6.4 oz.) 636g UPC
Recalled by Champion Foods, LLC
potential salmonella contamination
CLASS II Voluntary: Firm initiated
FDA record ↗

💊 Drug Recalls

20 active in the past 90 days · FDA Drug Enforcement
Jul 8, 2026
D-0690-2026
BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol),
Recalled by CareFusion 213, LLC
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicat
CLASS II Voluntary: Firm initiated
FDA record ↗
Jul 5, 2026
D-0689-2026
CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials,
Recalled by Chiesi USA, Inc.
Lack of Assurance of Sterility
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 28, 2026
D-0661-2026
Cinacalcet Hydrochloride Tablets, 30 mg, 30-count bottle, Rx Only, Manufactured by: Cipla
Recalled by Cipla USA, Inc.
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 28, 2026
D-0676-2026
Cinacalcet Hydrochloride Tablets, 90 mg, 30-count bottle, Rx Only, Manufactured by: Cipla
Recalled by Cipla USA, Inc.
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 28, 2026
D-0675-2026
Cinacalcet Hydrochloride Tablets, 60 mg, 30-count bottle, Rx Only, Manufactured by: Cipla
Recalled by Cipla USA, Inc.
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 25, 2026
D-0660-2026
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate
Recalled by Lannett Company Inc.
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0680-2026
QC Quality Choice, Carbamide Peroxide, 6.5%, 0.5 FL. OZ. (15 mL) a) Washer Bulb included (
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0679-2026
Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0685-2026
LEADER, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit -1 RUBBER BULB SYRINGE, 0.5 FL
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0683-2026
FAMILY Wellness, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), Kit - Washer Bulb Included, (
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0688-2026
CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0687-2026
meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0678-2026
CVS Health, Carbamide Peroxide, 6.5%, 0.5 FL Oz (15 mL), a) Bottle (NDC 51316-822-00.); b)
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0681-2026
TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS IN
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0682-2026
AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb Incl
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0684-2026
GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit - Washer Bulb I
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 24, 2026
D-0686-2026
Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distribute
Recalled by Bell Pharmaceuticals, Inc
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 23, 2026
D-0672-2026
Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous
Recalled by Reliance Life Sciences Private Limited
Lack of Sterility Assurance
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 23, 2026
D-0673-2026
Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcut
Recalled by Reliance Life Sciences Private Limited
Lack of Sterility Assurance
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 23, 2026
D-0671-2026
Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous
Recalled by Reliance Life Sciences Private Limited
Lack of Sterility Assurance
CLASS II Voluntary: Firm initiated
FDA record ↗

🩺 Medical Device Recalls

20 active in the past 90 days · FDA Device Enforcement
Jun 29, 2026
Z-2725-2026
Rapid Refill Continuous Injection System, UPN M00566001
Recalled by Boston Scientific Corporation
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe lo
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 15, 2026
Z-2644-2026
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer;
Recalled by Accuray Incorporated
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operat
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 15, 2026
Z-2640-2026
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer;
Recalled by Accuray Incorporated
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operat
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 11, 2026
Z-2746-2026
ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of
Recalled by Tosoh Bioscience Inc
The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated I
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2682-2026
ABIOMED Impella CP Set, Pump Set Code 0048-0003, containing BIOMED Impella Introducer, 14
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2685-2026
ABIOMED Impella CP Introducer Kit 14 Fr, 13 cm, Pump Set Code 0052-0038, containing Kit, 1
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2683-2026
ABIOMED Impella CP Introducer Kit 14 Fr, 13 and 25 cm, Pump Set Code 1000550, containing K
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2692-2026
ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP; containing Introducer Product
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2689-2026
ABIOMED Impella CP Set, Pump Set Code 0048-0014; containing Introducer Product Code 0052-3
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2686-2026
ABIOMED Impella CP Introducer Kit 14 Fr, 25 cm, Pump Set Code 0052-0039, containing Kit, 1
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2688-2026
ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460; containing In
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2681-2026
ABIOMED Impella RP Flex with SmartAssist Set, Pump Set Code 1000323, containing Kit, 23Fr
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2691-2026
ABIOMED Impella CP Set, Pump Set Code 0048-0044; containing Introducer Product Code 0052-3
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2687-2026
ABIOMED Impella 5.5 Smart Assist Set, JP, Pump Set Codes 1000211, 1000212; containing Intr
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2693-2026
ABIOMED Intro Kit, 14Fr x 13 and 25 cm, PKGD, JP, Pump Set Code 0052-0023-JP; containing I
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2690-2026
ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-0024-JP; containing Introducer
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 10, 2026
Z-2684-2026
ABIOMED Introducer Kit 23 Fr, 11 cm, Pump Set Code 1000441, containing Kit, 23Fr Introduce
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
CLASS I Voluntary: Firm initiated
FDA record ↗
Jun 9, 2026
Z-2729-2026
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/
Recalled by Orthofix U.S. LLC
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was la
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 9, 2026
Z-2723-2026
ICU Medical Plum Duo Infusion Pump, v1.2.3: 1) Item Number 400020401 and 2) Item Number
Recalled by ICU Medical, Inc.
In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and
CLASS II Voluntary: Firm initiated
FDA record ↗
Jun 9, 2026
Z-2678-2026
Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer Syste
Recalled by Oscor Inc.
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, und
CLASS I Voluntary: Firm initiated
FDA record ↗

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