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. 1,137 recalls have been distributed to Illinois in the last 12 months.
Showing 14621–14640 of 55,304 recalls
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arcos Modular Revision Hip System Recalled by Biomet, Inc. Due to The...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavitrackER Kit A: Knee Recalled by Orthosoft, Inc. dba Zimmer CAS Due to...
The Issue: The product was released for distribution without passing sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Luer Lok Access Device - intended as a sterile Recalled by...
The Issue: May shed contaminant particles into the urine specimen that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X (Product Number 781356) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X (Product Number 781358) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marketside 12oz Classic Salad SKU: 3107 Recalled by Dole Fresh Vegetables...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole 24oz Value Size Garden Salad SKU: 2109 Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kroger 12 oz Veggie Blend SKU: 3013 Recalled by Dole Fresh Vegetables Inc...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole 12oz Garden Salad / Salade Du Jardin SKU: 2673 Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: President's Choice 13oz Southwest Salad Kit / Le Choix du Recalled by Dole...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Presidents Choice 12 oz Garden Salad / Le Choix du Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.