chemical hazard Recalls

Abiomed Purge Cassette Recall 2026: 33,107 Impella Pump Sets Worldwide Over Purge Leaks

Increased risk of purge leaks with Generation 1 purge cassettes.

Mentor Artoura Breast Tissue Expanders Recall for Dull Needle Tips (2026)

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Mentor CPX 4 Breast Tissue Expanders Recalled in 2026 for Dull Needle Tip Hazard

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

XTANT Medical Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm Recalled for Mislabeling of Screw S

Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.

Kirkman MAXIMUM Zone 1 4% Lidocaine Cream Recall 178 Bottles (2026)

Stability Data Does Not Support Expiry Date.

Kirkman MAXIMUM ZONE 2 4% Lidocaine Cream Recall for Expiry Stability Issue (2026)

Stability Data Does Not Support Expiry Date.

Nilotinib Capsules Recall Expands in 2026 Over Stability Issue (Cipla USA)

Cipla USA recalls 271 cartons of Nilotinib 150 mg capsules nationwide after stability tests show out-of-spec results. The issue affects description and appearance by visual inspection. Stop using and contact Cipla USA or a clinician for guidance.

Molded Products MPC-130 See Luer Cap Set Recalled for High-Risk Assembly Issue (2026)

Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.

Medline Airway Exam Kit Recalled for 14,379 Units Over Olympus Valve Detachment (2026)

Medline ENFIT G-Tube Connector ENFIT1010GC Recalled for Leakage Risk (651,789 Units, 2026)

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.

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.

Medline Puracol Collagen Wound Dressings Recalled for Elevated Endotoxin Levels (2026)

Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic effects such as fever and hypotension. In severe cases, septic shock may result.

Boston Scientific EndoVive PEG Kit Recalled for Sterility Risk in 806 Kits (2026)

LEO Pharma Recalls Adbry Injection Over Sterility Concerns

Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.

VERGANI 1944 MILANO Pandoro Classico Gluten Free Recalled by Italianway Import (60 Units)

Potential contamination with foreign material (Teflon fragments) from flaking cooking molds.

SLADE GORTON Recalls Salmon Over Listeria Contamination

SLADE GORTON & CO. recalled 190 cases of Wellsley Farms Atlantic Salmon on February 10, 2026. The product may contain Listeria monocytogenes, a serious health risk. Consumers should not consume this product and seek a refund or replacement.

H & N Group Recalls Frozen Shrimp Over Cesium-137 Risk

H & N Group recalled 378 cases of frozen cooked shrimp on February 9, 2026. The product may be contaminated with Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume the shrimp and seek refunds.