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. 2,673 recalls have been distributed to Michigan in the last 12 months.
Showing 9221–9240 of 29,286 recalls
Recalled Item: BF-XT160 EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-3C40 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-1T180 EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atomlab 500 Dose Calibrator Software 2.0.00 through Revision 2.0.08 Recalled...
The Issue: When deleting a previously entered custom isotope, the software deletes the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-XP60 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Azurion series (within the limits of the used Operation Recalled by...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imperative Care Recalled by IMPERATIVE CARE INC Due to There is a potential...
The Issue: There is a potential for distal end of catheters to fracture and become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...
The Issue: Revised Instructions for Use: Potential for specimens from patients with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring Recalled by Greiner...
The Issue: Blood collection tubes may experience a clotting issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretch Leveller Model Number: 3156200 - The combination of this Recalled by...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Recalled...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.