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. 921 recalls have been distributed to Michigan in the last 12 months.
Showing 49281–49300 of 53,342 recalls
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...
The Issue: Siemens has discovered through product monitoring a potential malfunction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach...
The Issue: Product did not reach expected sterility assurance level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...
The Issue: Multiple studies were missing at a customer location that never made it to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Glenosphere orientation guide Product Usage: The glenosphere...
The Issue: The Glenosphere Orientation Guide Instrument Used with the Delta XTEND...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PadPro(R) Adult Radiotransparent Multifunction Electrodes Recalled by ConMed...
The Issue: ConMed was notified by the contract manufacturer that their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pure-Aid Allergy Relief Recalled by Kareway Product Inc Due to Labeling: Not...
The Issue: Labeling: Not Elsewhere Classified; foil label on immediate blister pack...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: - Average Medium Blade 9mm x 25mm x 0.38mm Ref. 2296-3-111 Lot 122590...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TPS Micro Reciprocating Small Tear Cross Cut Rasp 5.0mm x Recalled by...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Cannulated Drill Bit for Mini TightRope Ref. AR-8911DC Lot Recalled by...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Abrader Bur Recalled by Surgical Instrument Service And Savings, Inc. Due...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - ENDOPATH Resposable Bladeless Trocar Recalled by Surgical Instrument...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - ACCU-PASS Suture Shuttle Recalled by Surgical Instrument Service And...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -90 Degree L-Hook Tip Arthroscopic Electrode Recalled by Surgical Instrument...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.