Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,823 recalls have been distributed to Minnesota in the last 12 months.
Showing 40641–40660 of 52,120 recalls
Recalled Item: E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized Recalled by...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : Recalled by...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) W/V (weight/volume) VERSABASE [4714] 0.05% (0.5MG/ML)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Domperidone BP Recalled by Freedom Pharmaceuticals Inc Due to Penicillin...
The Issue: Penicillin Cross Contamination: Potential for products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : Recalled by...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST CP 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) : PROGESTERONE : DHEA (Dehydroepiandrosterone Micronized) W/V...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fomepizole Injection Recalled by Navinta LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility. A recent FDA inspection reported GMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAGNETOM systems Aera/Skyra/Avanto/Verio with software syngo MR D13A...
The Issue: The gradient output supervision was permanently turned off on the MAGNETOM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LR Telescoping Cantilever Arms (5/pk) and LL Telescoping Cantilever Arms...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replace Select Tapered TiU RP 4.3x11.5mm Recalled by Nobel Biocare Usa Llc...
The Issue: A material used in the packaging of the dental implants may impart a sticky...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 Recalled by Specialty...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HTM Mechanism Set Set 16 Recalled by Specialty Appliance Works, Inc. Due to...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herbst Universal Nut which is used in a Herbst Appliance Recalled by...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.