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. 2,424 recalls have been distributed to Louisiana in the last 12 months.
Showing 44241–44260 of 51,202 recalls
Recalled Item: Pleo Fort SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not TABLETS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Recalled by McKesson Packaging Services Due to...
The Issue: Failed Dissolution Specification: Out of Specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIBERNET Embolic Protection System: Recommended Vessel Diameter 6.0 -7.0 mm...
The Issue: Medtronic is recalling a specific subset of lot numbers of the FIBERNET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIBERNET Embolic Protection System: Recommended Vessel Diameter 5.0 -6.0 mm...
The Issue: Medtronic is recalling a specific subset of lot numbers of the FIBERNET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIBERNET Embolic Protection System: Recommended Vessel Diameter 3.5 0 5.0 mm...
The Issue: Medtronic is recalling a specific subset of lot numbers of the FIBERNET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs...
The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer Recalled by Roche...
The Issue: electrode used beyond the guaranteed in-use 52 week lifetime,may leak and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...
The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.