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. 2,959 recalls have been distributed to Illinois in the last 12 months.
Showing 881–900 of 30,032 recalls
Recalled Item: Carescape B450 Recalled by GE Healthcare Finland Oy Due to Potential loss of...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator 11mm. Cranial Perforator. Recalled by Integra...
The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene...
The Issue: Zimmer Biomet is conducting a medical device recall for two (2) lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene...
The Issue: Zimmer Biomet is conducting a medical device recall for two (2) lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator 9mm. Cranial Perforator. Recalled by Integra...
The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...
The Issue: Although the etched length on the screw is correct, the length marked on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...
The Issue: Although the etched length on the screw is correct, the length marked on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Form Wrap: Back Recalled by DJO, LLC Due to The IFU (Information for...
The Issue: The IFU (Information for Use) on the wrap instructs the user to heat the hot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model: Incisive CT for Brazil SKD Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model: CT 5300 Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...
The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Recalled...
The Issue: Due to an identified manufacturing defect involving coating material lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model: Incisive CT Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...
The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...
The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...
The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.