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. 2,646 recalls have been distributed to Louisiana in the last 12 months.
Showing 11521–11540 of 29,201 recalls
Recalled Item: Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate...
The Issue: Incorrect lot number for Standard Oral Fluid Negative Calibrator on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are...
The Issue: Potential risk of brush detachment during cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...
The Issue: The plastic housing on the device may fracture
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Model: Ultimax-i Recalled by Canon Medical System, USA, INC. Due to...
The Issue: During a procedure, when images were acquired, and these images were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APPX 0.75ml Recalled by ICU Medical, Inc. Due to Identification of a...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7 IN (18CM) APPX 0.26ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 0.82 ml Recalled by ICU Medical, Inc. Due to Identification of a...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way Recalled by ICU Medical,...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 IN (33cm) APPX 0.96 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 IN(33cm) APPX 1.0 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.