Drug Recalls Center

Cipla Recalls Phytonadione Injectable Emulsion Due to Stability Issues

Failed Stability Specifications: Observed OOS results: eg results for colour index

Stryker MV3 Bariatric Bed Recalled Over Compatibility Issues

Stryker Medical recalled 286 MV3 bariatric beds on October 31, 2025. The beds may not be compatible with Arise 1000EX mattresses, posing risks to patients. Healthcare providers and patients must stop using the beds immediately.

Philips Recalls IntelliVue Patient Monitor Due to Alarm Failure

Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to alarm, posing serious risks to patients. Users must stop using the device immediately and follow the manufacturer's instructions.

Philips IntelliVue MX700 Recall Affects 1,913,441 Monitors Worldwide (2025)

Potential issue where the IntelliVue monitors did not alarm.

Dynashield Cream Recalled Due to cGMP Deviations

Dynashield, a 4 oz cream, is recalled after cGMP deviations were identified. The recall affects 7,944 units distributed nationwide. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

Dynashield Skin Protectant Recalled for cGMP Violations

Dynarex Recalls Wecare Calasoothe Ointment Over cGMP Violations

Trifecta Pharmaceuticals Recalls Clotrimazole Cream for cGMP Violations

Dynarex Recalls Moisturizing Wound Hydrogel Over cGMP Violations

Philips IntelliVue Patient Monitor MX800 Recalled for Alarm Failure

Potential issue where the IntelliVue monitors did not alarm.

Nivagen Zinc Oxide Ointment Recalled Due to cGMP Deviations

Blossom Pharmaceuticals Recalls Lanashield Skin Barrier Over cGMP Violations

Dynarex Recalls Zinc Oxide Ointment Over cGMP Deviations

Philips IntelliVue MX600 Patient Monitor Recall 2025 for Alarm Failure

Potential issue where the IntelliVue monitors did not alarm.

Philips IntelliVue M3002A Recall Over Alarm Failure Affects 1,913,441 Units (2025)

Potential issue where the IntelliVue monitors did not alarm.

PHILIPS IntelliVue MP80 Recall 1,913,441 Monitors Worldwide for Alarm Failure (2025)

Potential issue where the IntelliVue monitors did not alarm.

Stryker Recalls Arise 1000EX Mattresses Over Compatibility Issues

Stryker recalled 289 Arise 1000EX mattresses on October 31, 2025. The recall affects products sold nationwide due to potential incompatibility with MV3 beds. Users should stop using these mattresses immediately.

STRYKER NICO Myriad Handpiece Recall for 39,148 Units Worldwide (2026)

Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.

Philips IntelliVue MP40 Recall 1.9M Monitors Over Alarm Failure (2025)

Potential issue where the IntelliVue monitors did not alarm.

Dynarex Recalls Wecare Enema Due to Safety Violations

Dynarex Corporation recalled 18,912 containers of Wecare Enema on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately. The recall affects products distributed nationwide in the USA.

Philips IntelliVue MP50 Recall 2025 Over Alarm Failure in 1.9 Million Monitors

Potential issue where the IntelliVue monitors did not alarm.

Olympus HX-400U-30 Recall: 7,803 Endoscopic Ligation Devices Recalled in 2025

Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy.

B. Braun Medical Recalled 12,225,913 CARESITE IV Sets for Backflow, Occlusion (2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

B. Braun Medical CareSite IV Sets Recalled for Backflow Risk (381,850 Units, 2025)

Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).