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. 2,024 recalls have been distributed to Illinois in the last 12 months.
Showing 21341–21360 of 30,032 recalls
Recalled Item: BIOGRAPH 64-3R TruePoint Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH Sys 40-3R to 40-4R Recalled by Siemens Medical Solutions USA Inc....
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tryptic Soy Agar Recalled by Acumedia Manufacturers, Inc. Due to light...
The Issue: light precipitate may form in prepared plates of Acumedia Tryptic Soy Agar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model Recalled...
The Issue: The replacement HEPA Filters have been manufactured with sealant that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streamline OCT Occipito-Cervico-Thoracic System Recalled by RTI Surgical,...
The Issue: Potential for a product defect where the cannula may be obstructed. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...
The Issue: Potential for polystyrene particulate presence.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...
The Issue: Potential for polystyrene particulate presence.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH SYS 64-3R to 64-4R Recalled by Siemens Medical Solutions USA Inc....
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT-S(64) 4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT-S(40) 3R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...
The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...
The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Red Head 2 Reusable Fat Harvesting Canister Recalled by Miami Fat...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-slice SKD whole body computed tomography X-ray system. Imaging...
The Issue: The following issues have been found in MX 16-slice systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-slice whole body computed tomography X-ray system. Imaging diagnostic...
The Issue: The following issues have been found in MX 16-slice systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.