Search U.S. Product Recalls Database

Showing 6781–6800 of 8389 results

Sort:

INTERTAN Nail (Smith & Nephew) – left-right labeling error (2022)

Right nails were anodized, marked, and labelled as left nails and vice versa

FDAApr 22, 2022Nationwide• Smith & Nephew Orthopaedics GmbH Alemannenstr. 14 Tuttlingen Germany

Medline Enzymatic Cleaning Sponge (Medline) – microbial contamination (2022)

Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.

FDAApr 21, 2022Nationwide• MEDLINE INDUSTRIES, LP Northfield

Stay Informed

Search Product Recalls

INTERTAN Nail (Smith & Nephew) – left-right labeling error (2022)

Medline Enzymatic Cleaning Sponge (Medline) – microbial contamination (2022)

15 Liters Drain Bag (Baxter) – regulatory clearance issue (2022)

APD Drain Manifold (Baxter) – regulatory clearance issue (2022)

Medline Bedside Cleaning Kit (Medline) – microbial contamination (2022)

Effluent Sample Bag (Baxter) – regulatory clearance issue (2022)

Extension Set (Baxter) – regulatory clearance issue (2022)

5 Prong Manifold Set (Baxter) – regulatory clearance issue (2022)

Locking Cap (Baxter) – regulatory clearance issue (2022)

Medline Foam Bedside Kit (Medline) – microbial contamination (2022)

Atrium Thoracic Catheter (Atrium) – expiration date mismatch (2022)

Uretero-Reno Fiberscope (Olympus) – adhesive problem (2022)

Olympus Cystonephrofiberscope (Olympus) – adhesive problem (2022)

Cardioblate Gemini-s (Medtronic) – jaw tip fracture (2022)

Proteus235 Proton Therapy (Ion Beam) – scanning magnet issue (2022)

C304-HIS Device (Medtronic) – sterility barrier concern (2022)

GE Replacement Batteries (GE Healthcare) – backup power issue (2022)

GE Ventilator Batteries (GE Healthcare) – backup power issue (2022)

Medfusion Syringe Pump (Smiths Medical) – Therapy Interruption (2022)

Medfusion Syringe Pump (Smiths Medical) – multiple issues (2022)