Product Recalls in Illinois
Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,713 recalls have been distributed to Illinois in the last 12 months.
Showing 34081–34100 of 55,304 recalls
Recalled Item: MEVATRON KD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Influenza Transport Swab Packages Recalled by Quidel Corporation Due to...
The Issue: Quidel Corporation is recalling Influenza Transport Swab Packages because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6700 (MX) Accelerator Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Hospira Inc., A Pfizer...
The Issue: Presence of Particulate Matter: A hair was found stuck to the stopper of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...
The Issue: Potential glass inclusion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...
The Issue: Potential glass inclusion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...
The Issue: Potential glass inclusion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...
The Issue: Potential glass inclusion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass inclusion
The Issue: Potential glass inclusion
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Premier Guard Drape Recalled by Covidien LLC Due to Sterility compromised...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XTRAC Excimer Laser Recalled by Strata Skin Sciences, Inc. Due to When the...
The Issue: When the Liquid Guide ( LLG) is not used according to the operator manual,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) Recalled...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR450 The systems are whole body magnetic resonance scanners...
The Issue: Potential safety issue with the patient bore heating on the Discovery MR450...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cadence Total Ankle System Recalled by Integra LifeSciences Corp....
The Issue: Posterior tibial fractures have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CaviWipes1 Extra Large Recalled by Metrex Research, LLC. Due to Metrex is...
The Issue: Metrex is recalling the CaviWipes Extra Large because they may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW¿ Multi-Food 1 Tablets Recalled by NOW Foods Due to Product's supplement...
The Issue: Product's supplement fact panel incorrectly states that the product contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: glipiZIDE Extended-Release Tablets Recalled by Mylan Pharmaceuticals Inc....
The Issue: Presence of Foreign Tablets/Capsules; bottles of Glipizide 5 mg tablets may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.