stop use immediately Recalls

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall (2026)

CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall 2026 — 6 Packaging Sizes

CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution

AvKARE Recalls Amantadine HCl Capsules Over Dissolution Issues

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Erbe USA Recalls 2,408 Flexible Cryoprobes for Surgery Over Rupture Risk (2026)

Probes may rupture/burst during activation

Erbe USA Recalls 5,154 Flexible Cryoprobes for Surgical Use Over Rupture Risk (2026)

Erbe USA recalled 5,154 Flexible Cryoprobes used in surgery after probes may rupture during activation. The defect can cause rupture or burst during activation. Stop using the device and follow recall instructions from the manufacturer.

Olympus Endoscope Reprocessor OER-Elite Recall Affects 2,929 Units (2026)

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Olympus OER-Pro Endoscope Reprocessor Recall for 3,354 Units Over MAJ-1443/1444 Compatibility (2026)

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Erbe USA Recall 33,390 Flexible Cryoprobes Over Rupture Risk (2026)

Probes may rupture/burst during activation

Olympus MAJ-1444 Endoscope Air/Water Valve Recall 2026 for 89,579 Units

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Fortemotus Bed Rails Recalled Over Entrapment and Asphyxiation Risk

LShome Smoke Detectors Recalled Over Failure to Warn During Fire

LShome recalled 3-Pack Smoke Detector Fire Alarms on February 12, 2026, due to a failure to warn during a fire. The defect poses a serious risk of injury or death. Consumers should stop using these alarms immediately and contact the manufacturer for a refund.

Oregon Potato Company Recalls Blueberries Due to Listeria Risk

Eptifibatide Injection Recalled Over Labeling Error

Slate Run Pharmaceuticals recalled Eptifibatide Injection on February 12, 2026. The recall affects all lots of the 75 mg/100 mL vial due to incorrect dosing information. Healthcare providers and consumers must stop using the product immediately.

Burlington Medical Kilt Recall: 15,216 Units Worldwide Over Attenuation Degradation (2026)

Potential for attenuation degradation over time, decreasing the lifespan.

CareFusion 303 BD Alaris System with Guardrails Suite MX Recall Impacts 1,025,567 Units (2026)

Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units

Burlington Medical Frontal Aprons Recalled for Attenuation Degradation in 2026 (14,323 Units)

Potential for attenuation degradation over time, decreasing the lifespan.

Burlington Medical Half Aprons Recalled for Attenuation Degradation Risk (2026)

Potential for attenuation degradation over time, decreasing the lifespan.

Burlington Medical Recalled 15,438 Radiation Attenuation Vests Over Degradation Risk (2026)

Potential for attenuation degradation over time, decreasing the lifespan.

Burlington Medical Kilt Blockers Recalled 94 Units Worldwide for Attenuation Degradation (2026)

Potential for attenuation degradation over time, decreasing the lifespan.