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. 2,043 recalls have been distributed to Illinois in the last 12 months.
Showing 19661–19680 of 30,032 recalls
Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...
The Issue: A damaged temperature sensor at the endoscope's tip can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to It has been...
The Issue: It has been observed during testing that there could be clinically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II implantable drug infusion pump Recalled by Medtronic...
The Issue: Medtronic received a complaint that there was an error code displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...
The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...
The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....
The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raindrop Near Vision Inlay Recalled by Revision Optics Inc Due to ReVision...
The Issue: ReVision Optics has updated the instructions for use (IFU) for the Raindrop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.