Health & Personal Care Recalls

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.

Mentor Texas LP Recalls CPX 4 US Breast Tissue Expanders with Suture Tabs (2026)

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

Mentor Texas CPX 4 Breast Tissue Expander Recall 2026 for Dull Needle Tips

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.

K Kirkman FIVE-STAR VASOCAINE Spray Recall for Expiry-Date Stability Issue (2026)

Stability Data Does Not Support Expiry Date.

Nilotinib Capsules 200 mg Recall: 164 Cartons Nationwide in 2026

Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.

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.

Midodrine Hydrochloride Tablets Recall 8,892 Cartons Nationwide (2026)

Defective container; inadequately sealed blister packaging.

Medline Anterior Hip Pack Recall Affects 14,379 Kits With Olympus Biopsy Valves (2026)

Abiomed Impella Automated Controller Recall 62 Units in 2026

Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*) pumps.

Medline Recalls 14,379 Olympus Biopsy-Valve Kits in 2026

Medline recalls 14,379 Olympus biopsy valve kits over rubber fragments in 2026 recall

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

Olympus Biopsy Valves in Medline Thoracic Robotic Kits Recalled for Rubber Fragments (14,379 Kits,

Medline Recalls 14,379 Olympus Biopsy Valve Kits in 2026

Medline Industries Recalls 14,379 Olympus Biopsy Valve Kits for Rubber Fragments (2026)