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. 2,441 recalls have been distributed to Michigan in the last 12 months.
Showing 45641–45660 of 53,342 recalls
Recalled Item: Artis Zee Angiographic x-ray systems. Recalled by Siemens Medical Solutions...
The Issue: An inappropriate cable connection was assembled for certain Artis zee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger PS500 Power Supply Unit of the Infinity ACS Workstation Recalled by...
The Issue: The battery capacity of the optional PS500 Power Supply Unit of the Infinity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis Systems Product usage: Artis zee is a family Recalled by Siemens...
The Issue: Certain units of the AXIOM Artis Systems are using a flat detector cooling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to Potential safety...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Infinia and Infinia Hawkeye Nuclear Medicine Systems. For...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMP X-alt Acetabular Liner This acetabular liner is intended for Recalled by...
The Issue: Packaging error -- two different types and sizes of acetabular liners used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MORPH ACCESSPRO Steerable Introducer Recalled by Biocardia, Inc. Due to...
The Issue: Tyvek packaging may be worn, causing loss of package integrity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips HeartStart FR3 Automated External Defibrillator (AED) Recalled by...
The Issue: Philip's is recalling HeartStart FR3 Automated External Defibrillator (AED)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...
The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...
The Issue: Incorrect master label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...
The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...
The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.