Product Recalls in Michigan
Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,463 recalls have been distributed to Michigan in the last 12 months.
Showing 43721–43740 of 53,342 recalls
Recalled Item: METOCLOPRAMIDE ORAL SOLUTION Recalled by VistaPharm, Inc. Due to Defective...
The Issue: Defective Container: Product leaks when inverted.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROPRANOLOL HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due...
The Issue: CGMP Deviations: Citations given to API supplier by the Italian Health...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: McCormick Ground Oregano in 0.75 oz plastic bottle. NUMBER: Recalled by...
The Issue: Retail sample of ground oregano tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AXIOM Luminos dRF system with SW VD10 or on Luminos Recalled by Siemens...
The Issue: It was determined that a potential malfunction may occur on the Luminos dRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eXpertDC intraoral x-ray Recalled by Gendex Corp Due to Two (2) failures of...
The Issue: Two (2) failures of the spring link components within the articulated arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model...
The Issue: The device may have a non-conforming component that may cause the device to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Titamax WS Cortical Implant ¿4.0 x 5 mm (Endosseous Recalled by...
The Issue: Product not approved for use in the US
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENVOY 500 AST Reagent Kit Recalled by ELITech Clinical Systems SAS Due to...
The Issue: Some users of ENVOY 500 AST Reagent Kit, 55255, for Envoy 500 systems are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Magnesium RTU Reagent Recalled by Horiba Instruments, Inc dba...
The Issue: Horiba Medical is recalling the ABX PENTRA Magnesium RTU Reagent because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rejuvenator Chamber manufactured by Baro-Therapies Recalled by...
The Issue: The firm is distributing the Rejuvenator device without an approved 510(k).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Respiratory Modules E-sCO Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.