Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,727 recalls have been distributed to Louisiana in the last 12 months.
Showing 50561–50580 of 51,202 recalls
Recalled Item: Covidien ROTICULATOR 30-4.8 Single Use Stapler REF# 017617 The RETICULA...
The Issue: Potential for the sterility barrier to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT- DR HENDRICKSO Product Usage: The Sarns Cardioplegia...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien ROTICULATOR 30-3.5 Single Use Stapler REF# 017615 The RETICULA...
The Issue: Potential for the sterility barrier to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch Recalled by...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT- DR.VAN TRIGHT. The Sarns High Flow Aortic Recalled by...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien ROTICULATOR 55-3.5 Single Use Stapler REF# 017612 The RETICULA...
The Issue: Potential for the sterility barrier to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 6.7 MM (20 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien ROTICULATOR 55-4.8 Single Use Stapler REF# 017614 The RETICULA...
The Issue: Potential for the sterility barrier to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED FX25RW H/L PACK Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dent's Extra Strength Toothache Gum Recalled by Grandpa Brands Co Due to...
The Issue: Superpotent; benzocaine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The product has the Catalogue/Part number 60010. Olympic Cool-Cap System...
The Issue: The Olympic Cool-Cap's Control Module has experienced a frozen screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...
The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Recalled by Hill...
The Issue: Subpotent; fluocinolone acetonide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Topical Oil (Scalp Oil)...
The Issue: Subpotent; fluocinolone acetonide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morton Recalled by Morton Salt Co. Due to Impurities/Degradation Products:...
The Issue: Impurities/Degradation Products: The product was found to contain a slightly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panera Recalled by Panera Bread LLC Due to Product ingredient statement...
The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Oysters Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...
The Issue: Korean Certified Shippers delisted from ICSSL.
Recommended Action: Do not consume. Return to store for a refund or discard.