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. 1,872 recalls have been distributed to Minnesota in the last 12 months.
Showing 30161–30180 of 52,120 recalls
Recalled Item: VenomX Recalled by Phillips Co. Due to GMP Deviations; FDA inspection found...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume) Recalled...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tetracycline-ABC Brand Topical ointment First Aid Antibiotic Recalled by...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diabecline brand Topical Ointment First Aid Antibiotic Recalled by Phillips...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect diabetes management software app Recalled by Roche...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Code: LM290 Recalled by Wicks Due to Undeclared Milk
The Issue: The firm's breaded seafood products were breaded using an ingredient, which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Code: 425FS Recalled by Wicks Due to Undeclared Milk
The Issue: The firm's breaded seafood products were breaded using an ingredient, which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WICK'S (4) Oven-Ready Recalled by Wicks Due to Undeclared Milk
The Issue: The firm's breaded seafood products were breaded using an ingredient, which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gourmet Bay - Toasted Crumb Breaded Tilapia Recalled by Slade Gorton &...
The Issue: Products recalled due to undeclared allergen -milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gourmet Bay - Citrus Coconut Breaded Tilapia Recalled by Slade Gorton &...
The Issue: Products recalled due to undeclared allergen -milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gourmet Bay - Honey Mustard Breaded Tilapia Recalled by Slade Gorton &...
The Issue: Products recalled due to undeclared allergen -milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core (Model No. 728321) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 (Model No. 728323) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 (Model No. 728231) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP (Model No. 728311 Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Oncology CT (Model No. 728243) software version Recalled...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.