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. 2,506 recalls have been distributed to Louisiana in the last 12 months.
Showing 28201–28220 of 51,202 recalls
Recalled Item: BO-TOP 20705 SMALL PATIENT 1/4 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 41201 ECC 3/8 PUMP PAC Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 24500 ADULT ECC Recalled by Datascope Corporation Due to The Better...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-T 9410 Lurie Chldns Small 1/4 Recalled by Datascope Corporation Due to...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 8504 1/4X1/4 PACK W/QP Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 25500 ECC 3/8 w/QiD Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 40700 HUNTINGTON Recalled by Datascope Corporation Due to The Better...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 5210 ECC Set - Respiratory Recalled by Datascope Corporation Due to...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BO-TOP 20700 SMALL PATIENT 3/8 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECC Small - Respiratory BEQ-TOP 5210 Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BO-TOP 13901 RAPID RESPONSE Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Patient ECC Pack BEQ-TOP 22301 Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult ECC Pack BEQ-TOP 22300 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 33700 ECC 3/8" PACK Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22301 Recalled by Datascope Corporation Due to The Better Bladder...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bliss anti-stress formula Dietary Supplement Recalled by Market America Inc...
The Issue: Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...
The Issue: Teleflex is recalling these products because the jaws of the tool tip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.