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. 2,387 recalls have been distributed to Minnesota in the last 12 months.
Showing 44961–44980 of 52,120 recalls
Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...
The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...
The Issue: There is a potential for communication loss associated with the F5-01 Frame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compensator Slider Lambda 6x20 component (part number 473704-0000-000)...
The Issue: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...
The Issue: Potential for unexpected heating of the transformer mounting bolt located...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINERAL IV Injection Recalled by Abrams Royal Pharamacy Due to...
The Issue: Non-Sterility; analytical results found product to contain Sphingomonas...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Unexpired Sterile Drug Products Recalled by Abrams Royal Pharamacy Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thickened Water Nectar Thick 32 oz. (944ml) Phase 1 Ingredients: Recalled by...
The Issue: NUTRA Balance Thickened Water Nectar Thick was found by the FDA to contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thickened Water Pudding Thick 32 oz. (944ml) Phase 3 Ingredients: Recalled...
The Issue: NUTRA Balance Pre-Thickened Water was found to contain mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...
The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...
The Issue: STERIS has identified that the outer shipping package for one lot (Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...
The Issue: Three problems were reported to the firm: When positioning for a relative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...
The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...
The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.
The Issue: Sterility cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.
The Issue: Sterility cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benefiber fiber supplement stick packs Recalled by Novartis Consumer Health...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.