Bard Access Systems, Inc. recalls OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 01108
See all recalls from Bard Access Systems, Inc. →Recalled Product
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI Code: 0110885403108365 TPT1000 THORACENTESIS/PARACENTESIS TRAY UDI-DI Code: 0110885403108488 The Acute Drainage devices are indicated for use in removing fluid from either the pleural or peritoneal spaces during an acute drainage / aspiration procedure.
Hazard / Issue
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Issued by
FDA
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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Search Amazon for OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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