Drug Recalls Center

514 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.

514
Total Drug Recalls
24
High Risk Medications
FDA
Official Source

Important Medication Safety Information

  • Do not stop taking prescribed medications without consulting your healthcare provider
  • Contact your pharmacist or doctor if you have a recalled medication
  • Check lot numbers carefully - not all batches may be affected
  • Return recalled medications to your pharmacy for proper disposal

Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.

HIGHFDA DEVICE

DJO Surgical Recalls Reamer Head Due to Binding Hazard

DJO Surgical recalled 927 units of the Altivate Reverse Wedge Glenoid Reamer Head on July 18, 2025. The recall follows reports that the device may kick or bind up during use. Healthcare providers and patients must stop using the product immediately.

DJO Surgical
Their is
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HIGHFDA DEVICE

DJO Surgical Recalls Glenoid Reamer Sleeve Due to Kickback Risk

DJO Surgical recalled 447 units of the Altivate Reverse Wedge Glenoid Reamer Sleeve on July 18, 2025. The recall follows reports that the device may kick or bind during use, presenting a serious hazard to patients. Healthcare providers and patients should discontinue use immediately and follow the manufacturer's instructions.

DJO Surgical
Their is
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HIGHFDA DRUG

DermaKleen Antiseptic Lotion Soap Recalled for Microbial Contamination

DermaRite Industries LLC recalled 11,321 bags of DermaKleen antiseptic lotion soap on July 17, 2025. The product, contaminated with Burkholderia cepacia, poses a serious health risk. Consumers should stop using the product immediately and contact health providers for guidance.

DERMAKLEEN
Microbial Contamination
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HIGHFDA DRUG

DermaSarra Analgesic Recalled Due to Microbial Contamination

DermaRite Industries LLC recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025. The product contains camphor and is contaminated with Burkholderia cepacia. This recall is classified as Class I due to the potential health risks.

DERMASARRA
Microbial Contamination
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HIGHFDA DEVICE

C.R. Bard Recalls Foley Catheter Trays Over Allergy Risk

C.R. Bard recalled 3,670 Foley catheter trays on July 17, 2025, due to incorrect inserts. Users may confuse materials, leading to allergies or infections. Healthcare providers and patients must stop using these trays immediately.

C.R. Bard
Foley catheter
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HIGHFDA DEVICE

C.R. Bard Recalls Foley Catheter Trays Over Allergy Risk

C.R. Bard recalled 4,300 Foley catheter trays on July 17, 2025. Incorrect inserts may lead users to misidentify materials, increasing infection and allergic reaction risks. Patients and healthcare providers must stop using the trays immediately and follow recall instructions.

C.R. Bard
Foley catheter
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HIGHFDA DEVICE

C.R. Bard Recalls Foley Catheter Tray Over Infection Risk

C.R. Bard Inc issued a recall for 4,300 Foley catheter trays on July 17, 2025. Incorrect inserts lead to potential allergic reactions and infection risk. Healthcare providers and patients must stop using the device immediately.

C.R. Bard
Foley catheter
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HIGHFDA DRUG

DermaRite Recalls KleenFoam Soap Over Microbial Contamination

DermaRite Industries recalled 6,973 cartridges of KleenFoam Antimicrobial Foam Soap on July 17, 2025. The product contains a harmful bacterial contamination, Burkholderia cepacia. Consumers should stop using the soap immediately and seek guidance from healthcare providers.

KLEENFOAM
Microbial Contamination
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HIGHFDA DEVICE

Stryker Surgical Light System Recalled Over Chipping Hazard

Stryker Communications recalled 40 surgical light systems on July 15, 2025, due to potential powder coating chipping. This defect increases risks for healthcare providers and patients. Affected products were distributed nationwide, including Texas, Illinois, and New York.

Stryker Communications
Surgical lights
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HIGHFDA DRUG

Boothwyn Pharmacy Recalls Fluorescein 2% Ophthalmic Solution

Boothwyn Pharmacy recalled 8 vials of Fluorescein 2% Ophthalmic Solution on July 9, 2025. The recall occurred due to the drug being subpotent, posing potential health risks. Consumers should stop using the product immediately and seek guidance from their healthcare provider.

Boothwyn Pharmacy
Subpotent Drug
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HIGHFDA DRUG

Boothwyn Pharmacy Recalls Semaglutide Injection for Subpotency

Boothwyn Pharmacy recalled 642 vials of Semaglutide injection on July 9, 2025. The recall follows the discovery that the drug is subpotent. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Boothwyn Pharmacy
Subpotent Drug
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HIGHFDA DEVICE

Boston Scientific Recalls Deep Brain Stimulation Devices Over Wire Break Risk

Boston Scientific Neuromodulation recalled 25,260 deep brain stimulation systems on July 8, 2025, due to wire break issues. Users may experience loss of therapy and other serious complications. Patients should stop using the devices immediately and seek further instructions.

Boston Scientific Neuromodulation
Wire break(s)
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HIGHFDA DRUG

Medline Alcohol Prep Pads Recalled Due to Subpotent Alcohol Levels

Medline Industries recalled approximately 6.67 million alcohol prep pads on July 7, 2025. The recall stems from isopropyl alcohol levels falling below the labeled concentration. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Medline Alcohol Prep
Subpotent Drug-
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HIGHFDA DEVICE

Tandem Diabetes Care Recalls t:slim X2 Insulin Pump Over App Issues

Tandem Diabetes Care recalled 19 t:slim X2 Insulin Pumps on July 3, 2025, due to an app defect. The defect affects devices when set to right-to-left languages, potentially causing incorrect therapy decisions. This may lead to hypoglycemia or hyperglycemia.

Tandem Diabetes Care
an app
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