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. 2,011 recalls have been distributed to Illinois in the last 12 months.
Showing 23781–23800 of 30,032 recalls
Recalled Item: 104" (264 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 113" (287cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 107" (272 cm) Ext Set w/2 Check Valves Recalled by ICU Medical, Inc. Due to...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Systems LOCI Thyroid Stimulating Hormone Recalled by Siemens...
The Issue: Dimension Vista LOCI Thyroid Stimulating Hormone (TSH) Lot 14237AA may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...
The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...
The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...
The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GMK Hinge knee prosthesis Recalled by Medacta Usa Due to Incorrect parts:...
The Issue: Incorrect parts: Packages of the GMK Hinge Tibial Augmentation size 4-10 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delivery/C-Section Recalled by Covidien LLC Due to Devon Light Gloves...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered HD Upgrade Set Recalled by BioHorizons Implant Systems Inc Due to...
The Issue: BioHorizons Tapered HD Upgrade set was packaged with an incorrect drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minor Surgical Kits Recalled by Covidien LLC Due to Devon Light Gloves...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASC (Breast) Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Basin Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.