Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,548 recalls have been distributed to Mississippi in the last 12 months.
Showing 18301–18320 of 28,172 recalls
Recalled Item: The PreludeSYNC Radial Compression Device is a sterile Recalled by Merit...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Item Code: 91650 The sterile eye Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Sodium Chloride Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Item Code: 03201 The sterile eye Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm) Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...
The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed that in isolated cases when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance Peripheral Guide Wire with Flex Tip Recalled by...
The Issue: Cardiovascular Systems, Inc. is recalling one lot of ViperWire Advance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: It is recommended for patients with weight/size between 4-22 lbs Recalled by...
The Issue: Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Oval Recalled by Covidien LLC Due to Product...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.