Health & Personal Care
HIGH
FDA DEVICE
CPM Medical Consultants Recalls 3,317 Fuse ULTRA Foot Plating System IFU Updates (2025)
CPM Medical Consultants
Instructions for
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 DEVICE
Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.
Baxter Healthcare
Affected oral/axillary
Health & Personal Care
HIGH
FDA DEVICE
Percussionaire IPV In-Line Valve Recall Aims to Stop Use Over Leakage Risk in Ventilators
Percussionaire
IFU update;
Health & Personal Care
HIGH
FDA DRUG
Park Avenue Compounding Phenylephrine HCI Syringes Recalled Over CGMP Violations
Park Avenue Compounding
CGMP Deviations
Health & Personal Care
HIGH
FDA DEVICE
Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)
InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.
Enterix
InSure ONE
Health & Personal Care
HIGH
FDA DRUG
Accord Healthcare Recalls 54,432 Levothyroxine 88 mcg Tablets for Subpotent Potency (2025)
Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.
Levothyroxine Sodium
Subpotent: During
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella Automated Controller Recall Affects 9,177 Units Worldwide (2025)
Potential for Automated Impella Controller (AIC) purge pressure issues due to purge retainer failures.
Abiomed
Potential for
Health & Personal Care
HIGH
FDA DRUG
IntegraDose Oxytocin IV Solution Recall 2025 for Subpotent Drug, 853 Bags Nationwide
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
IntegraDose Compounding Services
Subpotent Drug:
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DRUG
Carbamazepine Extended-Release 400 mg Tablets Recalled for Failed Dissolution Specifications (D-0675
Carbamazepine
Failed Dissolution
Health & Personal Care
HIGH
FDA DEVICE
FUJIFILM Healthcare CH-200 Recalled for Broken X-ray Tube Shaft in 16 Units
It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was broken while being operated toward the front while lifting.
FUJIFILM Healthcare
It was
Health & Personal Care
HIGH
FDA DRUG
Graviti Pharmaceuticals Bupropion Hydrochloride XL 300 mg Recall Impacts 46,512 Bottles (2025)
Bupropion Hydrochloride
Failed Tablet/Capsule
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Inc. Benzoyl Peroxide Cleanser Recalled for Benzene Contamination (2025)
Private Label Skin Care Inc. recalled edunn clarity BP Treatment Cleanser 10% after benzene was detected. The recall covers lot numbers 58170A and 58172A with expiration September 2025. The product was distributed in California and Georgia.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Benzoyl Peroxide 10% Recall for Benzene Contamination
Private Label Skin Care recalls Artisan of Skin Benzoyl Peroxide 10% cream after benzene detected. The product was distributed in California and Georgia. Consumers should stop use immediately and contact the company for guidance.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Micronized Benzoyl Peroxide Gel Recall Expands for Benzene Contamination
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Skin MD Body Acne Cleanser Recalled for Elevated Benzene Levels (2025)
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Skin MD
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Torrey Pines Benzaderm BPO Cleanser 10% Recall Over Benzene Contamination, 2025
Torrey Pines Dermatology & Laser Center's Benzaderm BPO Cleanser recall remains active. The FDA-listed recall covers benzoyl peroxide cleanser lot numbers 58170A and 58172A with expiration 09/2025. Consumers should stop use and contact the recall coordinator.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Inc. Benzoyl Peroxide 10% Acne Treatment Recalled for Benzene Contamination
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies Recalls 2 uCT ATLAS MD CT X-ray Systems for Mechanical Interference Risk (2025)
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies
Third-party outer
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies Recalls 8 Shanghai United Imaging uCT 530 MD CT Scanners Over Interference Risk (24
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Shanghai United Imaging Healthcare
Third-party outer
Health & Personal Care
HIGH
FDA DEVICE
Shanghai United Imaging Healthcare CT X-ray System uCT 550 MD Recall for 22 Units in 2025
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Shanghai United Imaging Healthcare
Third-party outer
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies uMI 550 MD PET/CT Recalled for 95 Units Over Mechanical Interference Risk (2025)
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies
Third-party outer
Health & Personal Care
HIGH
FDA DEVICE
Shanghai United Imaging Healthcare uMI Panorama 35 MD PET/CT System Recalled for 4 Units (2025)
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Shanghai United Imaging Healthcare
Third-party outer
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies uEXPLORER MD PET/CT Recall for 2 Units in 2025
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies
Third-party outer
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