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. 2,492 recalls have been distributed to Michigan in the last 12 months.
Showing 39561–39580 of 53,342 recalls
Recalled Item: Barilla MEDIUM SHELLS Recalled by Barilla America NY, Inc. Due to Barilla...
The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Barilla PENNE Recalled by Barilla America NY, Inc. Due to Barilla America...
The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman Recalled by...
The Issue: Bella Rosa Grated Parmesan Cheese may contain undeclared egg lysozyme.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silhouette Lift brochure Silhouette Sutures are for use in midface Recalled...
The Issue: Silhouette Lift is recalling the Silhouette Suture brochure because it does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zero Xtreme High Performance Fat Burner capsules Recalled by XTREME Z...
The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iovera 155 Smart Tip Recalled by Myoscience Inc Due to The expiration date...
The Issue: The expiration date on the outer box label and the pouch label for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Base CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Acetaminophen reagents Recalled by Siemens Healthcare...
The Issue: A change in the concentration of N-acetylcysteine (NAC) that may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.