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. 2,033 recalls have been distributed to Louisiana in the last 12 months.
Showing 6621–6640 of 29,201 recalls
Recalled Item: Ventstar Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kit Coax 3 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs (1) 89-10529.04 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P)250 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs: (1) 89-10507.02 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia WT (P)180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventstar Coax Recalled by Draeger Medical, Inc. Due to Glued connections of...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist catheter is an intravascular micro axial...
The Issue: The Impella 5.5 pump experienced a heightened complaint rate for purge leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P)180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Set2Go Ventilation 12 (A) Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Seattle PAP Plus Recalled by Draeger Medical, Inc. Due to Glued connections...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Set Coax 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN)...
The Issue: Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RR Mechatronics Starrsed Control Level N ESR Control 4.6 ml Recalled by...
The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro...
The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.