Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 30621–30640 of 48,219 recalls
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: 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: 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: 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: 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: 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: 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: 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: Transpac¿ IV Monitoring Kit Recalled by ICU Medical, Inc. Due to 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.
Recalled Item: Expression MR IBP DPT Kit Recalled by ICU Medical, Inc. Due to 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.
Recalled Item: Cath Lab Kit W/30ML Flush Device for Monongalia General Hosp Recalled by ICU...
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: TRANSPAC¿ IV MONITORING KIT DISPOSABLE TRANSDUCER WITH BONDED STOPCOCK...
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: QUAD TRANSDUCER KIT WITH 03ML FLUSH DEVICE FOR LUBBOCK HEART HOSP. Recalled...
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: Double LINE SAFESET" KIT WITH 03ML FLUSH DEVICE FOR E.U.S.H.C. Recalled by...
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: MONITORING KIT WITH 03ML FLUSH DEVICE FOR CONCORD HOSP. Recalled by ICU...
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: TRIFURCATED DISPOSABLE TRANSDUCER KIT W/03ML FLUSH DEVICE FOR JOHNS...
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: TRIPLE MK W/03ML FLUSH DEVICE FOR UNIV OF PENN. HEALTH SYSTEMS Recalled by...
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: TRANSPAC¿ IV MONITORING KIT DISPOSABLE TRANSDUCER 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.
Recalled Item: CATH LAB KIT FOR ALBERT EINSTEIN M.C. Recalled by ICU Medical, Inc. Due to...
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.