cpsc regulated Recalls

B Braun Medical PERIFIX FX Epidural Tray Recalled for 0 Units in 2025

Potential for the lid of the catheter connector to be in the incorrect position.

Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025

CGMP Deviations: Market complaints received for gritty texture (grainy)

Park Avenue Compounding Phenylephrine HCI Syringes Recalled Over CGMP Violations

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.

Percussionaire IPV In-Line Valve Recall Aims to Stop Use Over Leakage Risk in Ventilators

Lipton Green Tea Citrus Recalled for Undeclared Sugar in 2,854 Cases (2025)

Undeclared sugar in finished product-primary package does not reflect the product inside bottle.

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.

Lawrence Wholesale Shrimp Cocktail Bowls Recalled for Cs-137 Contamination Risk (2025)

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)

IntegraDose Oxytocin IV Solution Recall 2025 for Subpotent Drug, 853 Bags Nationwide

Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.

Alcon CONSTELLATION Ultravit 10K & HyperVit 20K Recall for 28,323 Units (2025)

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.

Graviti Pharmaceuticals Bupropion Hydrochloride XL 300 mg Recall Impacts 46,512 Bottles (2025)

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 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 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.

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.

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 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.

Diagnostica Stago STA Liatest D-Di Recall 12,740 Units Worldwide in 2025

A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.

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.