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. 2,517 recalls have been distributed to Michigan in the last 12 months.
Showing 34841–34860 of 53,342 recalls
Recalled Item: Endoscopic Articulating Linear Cutter Recalled by Ethicon Endo-Surgery Inc...
The Issue: Quality control identified a component issue where the pinion gear in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Four Birthing Bed Model P3700 The primary packaging is Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The...
The Issue: Topcon discovered an anomaly with titration, only when EpM is turned on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible that a change to an Order Set will not be saved in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poppers brand Mozzarella Cheese Sticks Net Wt. 32 oz. (2 Recalled by...
The Issue: Monogram Appetizers is recalling Poppers Brand Mozzarella Cheese Sticks...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Molly's Kitchen Hotzzarella Cheese Sticks Recalled by Ajinomoto Windsor...
The Issue: Ajinomoto Windsor is recalling Cheese Sticks because it may be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...
The Issue: It was reported by a customer that RadSuite images are not appearing as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...
The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with software version VA48A-SP2 Recalled by Siemens...
The Issue: Due to an internal communication error between the firmware and the software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash with software version VA48A-SP2 Recalled by Siemens...
The Issue: Due to an internal communication error between the firmware and the software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge with software version VA48A-SP2 Recalled by Siemens...
The Issue: Due to an internal communication error between the firmware and the software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.