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. 2,498 recalls have been distributed to Michigan in the last 12 months.
Showing 37561–37580 of 53,342 recalls
Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to All lots of RAPIDFILL...
The Issue: All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog...
The Issue: The Mallinckrodt (Therakos) post-market monitoring process detected an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Concerto Basic Shower Trolley is intended for assisted hygiene care...
The Issue: Reports of the bolts connecting the stretcher to the hydraulic piston and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N. The Fukuda...
The Issue: A possible malfunction where a Short-term Battery Error message has appeared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Preservation System Signature Series PreBent Burs under the following...
The Issue: Metal shavings released from burs during use are due to contact between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zzang! Wowza Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy; and undeclared milk (cream declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Cashew Cow Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared sub-ingredient soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Marshmallows Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: This Kid Saves Lives Chocolate Chip #10858497004097 UPC# 858497004090...
The Issue: This Bar Saves Lives is recalling This Kid Saves Lives Chocolate Chip...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Holiday 4 pack Candy Bars Recalled by Zingerman's Candy Manufactory...
The Issue: Product recalled due to undeclared soy; and undeclared allergen milk (cream...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Original Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy and milk (butter declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each Recalled...
The Issue: Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oncentra External Beam - VMAT - Radiation therapy planning system Recalled...
The Issue: When using the option "Tumor Overlap Fraction" in VMAT planning it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuse 1C Colonoscope Recalled by EndoChoice, Inc. Due to The bending section...
The Issue: The bending section of the device may partially separate from the insertion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: arkray SPOTCHEM II Basic Panel - 1 Reagent test strips Recalled by Arkray...
The Issue: One lot each of SPOTCHEM II Basic PANEL-1 Reagent Test Strip and SPOTCHEM II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoCoil 3.0T GEM Flex Coil. The 3.0T GEM Flex coil Recalled by NeoCoil, LLC...
The Issue: Potential for higher than specified surface temperatures. Use of 3.0T GEM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way Red Latex Foley Catheter Recalled by C.R....
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.