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. 2,943 recalls have been distributed to Illinois in the last 12 months.
Showing 3861–3880 of 30,032 recalls
Recalled Item: L-CATH PICC S/L Peripherally Inserted Central Catheter Recalled by Argon...
The Issue: Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare...
The Issue: Improperly performed testing prior to release
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor PCA Syringe Pump Recalled...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...
The Issue: The tiller separates from the base/front caster assembly. If the knee walker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...
The Issue: The tiller separates from the base/front caster assembly. If the knee walker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon X-Ray Bone Densitometer (DXA) Models: Horizon-A Recalled by Hologic...
The Issue: Non-conformance pertains to electromagnetic compatibility requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autotome RX 20mm CUT WIRE Cannulating Sphincterotome Recalled by Boston...
The Issue: Foreign material may be present on the enclosed section of the cutting wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foam Protective Pouches Recalled by Medical Action Industries, Inc. 306 Due...
The Issue: The protective pouches were identified to have been improperly labeled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.