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. 2,678 recalls have been distributed to Louisiana in the last 12 months.
Showing 7361–7380 of 29,201 recalls
Recalled Item: FoundationOne Liquid CDx (F1LCDx) Recalled by Foundation Medicine, Inc. Due...
The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Gauge Disposable Trocars with Blunt Pushers for Use with Recalled by ENDO...
The Issue: No expiration dates printed on the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...
The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...
The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InPen Diabetes Management App Recalled by Companion Medical, Inc. Due to...
The Issue: Diabetes management app may crash immediately upon opening, while using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...
The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...
The Issue: There is a potential for separation at the male connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...
The Issue: The power backup battery, under certain conditions, may exhibit reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...
The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...
The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total...
The Issue: Due to tears reported tears in the cannula due to wear and tear stress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.