Health & Personal Care
HIGH
FDA DEVICE
C-RAD POSITIONING AB Recalls Catalyst Device Over Treatment Risks
C-RAD POSITIONING AB
Due to
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
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.
Health & Personal Care
HIGH
FDA DRUG
ibspot Taoscare Motion Sickness Patches Recalled Over NDA/ANDA Issue (2025)
Marketed Without an Approved NDA/ANDA
ibspot
Marketed Without
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma FentaNYL Citrate PF IV Injection Recall 2025 Over Labeling Errors
STAQ Pharma recalled FentaNYL Citrate PF IV injection nationwide after labeling left incorrect or missing lot and expiration dates. Healthcare providers must stop using the product immediately. STAQ Pharma will provide recall instructions by letter.
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
USV Private Olopatadine Eye Drops 0.1% Recalled in 8,952 Bottles (2025)
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
USV Private
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma Hydromorphone HCl PF 10mg/50mL IV Injection Recall for Labeling Errors (2025)
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma Ketamine Hydrochloride Injection 50 mL Recall for Labeling Errors (2025)
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
Fasenra Benralizumab Injection Recall: 916 Pre-Filled Syringes Over Sterility Concern (2025)
Lack of Assurance of Sterility:
Fasenra
Lack of
Health & Personal Care
HIGH
FDA DRUG
Rising Pharma Carbidopa/Levodopa/Entacapone Tablets Recall 2,064 Bottles Nationwide (2025)
Rising Pharma Holdings
Product mix
Health & Personal Care
HIGH
FDA DRUG
Viona Pharmaceuticals Recalls 13,080 Tavaborole Topical Solution 5% Bottles (2025 Recall)
Zydus Lifesciences
Discoloration -
Health & Personal Care
HIGH
FDA DRUG
Advanced Pharmaceutical Technology Recalls Testosterone Pellets Due to Contamination Risk
Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.
Advanced Pharmaceutical Technology
Lack of
HIGH
CPSC
Almpal Dissolved Oxygen Test Kits Recalled for Non–Child-Resistant Sulfuric Acid Packaging
This recall involves Almpal dissolved oxygen test kits. The test kits come in a cream-colored box bearing a white label with "Dissolved Oxygen Test Kit" and the manufacture date, batch number, and expiration date printed on it.
Almpal
The recalled
Health & Personal Care
HIGH
FDA DEVICE
ICU Medical IV Gravity Burette Sets Recalled for Missing Shut-Off Valve (2025)
ICU Medical recalls 23,203 IV gravity burette sets worldwide. The burette component is missing an internal shutoff valve, which can delay therapy, cause overdelivery, or allow air to be infused. Stop using the device and contact ICU Medical for instructions.
ICU Medical
IV Gravity
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella Controller Recall Aims to Address Cybersecurity Vulnerabilities Across 32 Product SK
Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC).
Abiomed
Potential cybersecurity
Health & Personal Care
HIGH
FDA DRUG
Church & Dwight Zicam Elderberry Medicated Fruit Drops Recalled for Label Mix-Up (21,912 Bottles, 0
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Zicam
Labeling: Label
Health & Personal Care
HIGH
FDA DRUG
Camber Ketorolac Tromethamine Injection Recall 2025 for Glass Particulates
Presence of Particulate Matter: Particulate matter identified as glass
Ketorolac Tromethamine
Presence of
Health & Personal Care
HIGH
FDA DEVICE
SHENZHEN ATOMSTACK TECHNOLOGIES Recalls Laser Products Over Safety Hazard
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
SHENZHEN ATOMSTACK TECHNOLOGIES
Lack of
Health & Personal Care
HIGH
FDA DEVICE
B BRAUN MEDICAL STREAMLINE BLOODLINE SET FOR DIALOG Recalled 1,298,454 Units (2025)
The potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.
B BRAUN MEDICAL
The potential
Health & Personal Care
HIGH
FDA DRUG
AFCO Hand Sanitizer 5515 Recalled for Methanol Risk Nationwide (2025)
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.
AFCO
cGMP deviations:
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland 718096 Zenition 50 Interventional X-Ray System Recalled in 2025
Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
Health & Personal Care
HIGH
FDA DRUG
Medline 222,800 Alcohol Prep Pads Recalled for Subpotent Drug (2025)
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.
Medline Industries
Subpotent Drug
Health & Personal Care
HIGH
FDA DRUG
Acella Doxycycline Hyclate 100 mg Recall 2025 for Dissolution Failure - 4,680 Bottles Nationwide
Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.
Doxycycline
Failed dissolution
Health & Personal Care
HIGH
FDA DRUG
Acuity Specialty Products Hand Sanitizer Recalled for Methanol Risk Due to Unperformed Component-LOT
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.
Acuity Specialty Products
cGMP deviations:
Health & Personal Care
HIGH
FDA DEVICE
Synthes 5.0mm IM Nail Screw Recalled for Labeling Error (2025)
Although the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged and labeled as 46mm, while 46mm screws were packaged and labeled as 42mm.
Synthes
Although the
Health & Personal Care
HIGH
FDA DRUG
Dr. Reddy's Succinylcholine Chloride Injection Recall 2025 — 571 Vials Over OOS Preservative Drop
Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.
Succinylcholine
Out-of-Specification (OOS)
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