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. 2,448 recalls have been distributed to Mississippi in the last 12 months.
Showing 31521–31540 of 49,744 recalls
Recalled Item: Brownwood Farms Jalapeno Cherry Salsa. 21oz glass bottles and 1 Recalled by...
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Jalapeno Cherry Butter. 12oz glass bottles and 1 gallon....
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurities/Degradation Specifications: out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurities/Degradation Specifications: out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mini Resupply Trauma Kit - Product Code 85-0835 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Range Trauma Kit ORG - Product Code 80-0213 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: USCG Boat Response Kit - Product Code 80-0353 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amphibious Trauma Kit - Product Code 85-0639 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Range Trauma Kit Hardcase - Product Code 85-0889 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aid Backpack Kit - Product Code 85-0917 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Range Trauma Kit - Product Code 85-1274 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess FE 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc....
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advance Trauma Kit - Product Code 85-0742 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: K-9 Trauma Field Kit - Product Code 80-0211 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc. Due...
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical, Inc....
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess 24 FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRANSPAC¿ IV BIFURCATED MONITORING KIT 72 INCH Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RIGHT HEART CATH LAB KIT FOR BAPTIST MEM. HOSP. Recalled by ICU Medical,...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.