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. 2,358 recalls have been distributed to Mississippi in the last 12 months.
Showing 48981–49000 of 49,744 recalls
Recalled Item: Nat Flv Beef FF Recalled by International Flavors & Fragrances, Inc Due to...
The Issue: Product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Natural Chicken Flavor Seasoning Recalled by International Flavors &...
The Issue: Product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Beef Recalled by International Flavors & Fragrances, Inc Due to Potential...
The Issue: Product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bean Sauce Seasoning Recalled by International Flavors & Fragrances, Inc Due...
The Issue: Product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nat Flavor Beef Marrow Recalled by International Flavors & Fragrances, Inc...
The Issue: Product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grilled Chicken Marinade Recalled by International Flavors & Fragrances, Inc...
The Issue: Product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nat Beef FF Recalled by International Flavors & Fragrances, Inc Due to...
The Issue: Product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GoBed+ . Model FL20E Beds are intended for medical purposes Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Rose Bed Model (FL14E) Beds are intended for medical Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MA204 Bed Model (FL25E) Beds are intended for medical Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 2 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 1 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 3 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 9 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 5 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.