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. 2,641 recalls have been distributed to Illinois in the last 12 months.
Showing 55261–55280 of 55,304 recalls
Recalled Item: 7.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Tulip Recalled by NuVasive Inc Due to The tulip portion of the screw...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitrack System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer...
The Issue: Zimmer CAS voluntarily conducted a retrospective recall of the Navitrack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. Recalled by...
The Issue: GE initiated a correction to the instructions/use due to the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory...
The Issue: Distribution of a product that did not meet specifications. (labeling error)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitrack¿ System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer...
The Issue: ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK-FS Recalled by...
The Issue: Ventana Medical System is initiating the recall of the BenchMark and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: popchips¿ Sea Salt & Vinegar Recalled by Sonora Mills Foods Due to The firm...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheddar Mini Rice Snacks under the following brand names: Fred Meyer...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: popchips¿ Cheddar Potato Recalled by Sonora Mills Foods Due to The firm...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.