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. 2,733 recalls have been distributed to Illinois in the last 12 months.
Showing 29941–29960 of 55,304 recalls
Recalled Item: Peanut Delight (8 oz. bag) Recalled by Colorado Nut Co Due to Undeclared Milk
The Issue: Undeclared milk in snack mix products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Nutty Granola (8 oz. bag) Recalled by Colorado Nut Co Due to...
The Issue: Undeclared milk in snack mix products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cashew Cranberry Cherry Jubilee (8 oz. bag) Recalled by Colorado Nut Co Due...
The Issue: Undeclared milk in snack mix products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frontier Trail Mix (4 oz. bag) Recalled by Colorado Nut Co Due to Undeclared...
The Issue: Undeclared milk in snack mix products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ECOLAB MICROTEK Rolled Probe Cover Recalled by ECOLAB INC Due to The...
The Issue: The incorrect IFU was shipped with the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: Recalled by...
The Issue: Component of the Lap-Band system was missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECOLAB MICROTEK Rolled Probe Cover Recalled by ECOLAB INC Due to The...
The Issue: The incorrect IFU was shipped with the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...
The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...
The Issue: It was discovered that the product units it imported may, at peak levels,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Teva...
The Issue: Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...
The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to When calculating...
The Issue: When calculating electron Monte Carlo dose with a very large number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDAN Telemetry Transmitter Recalled by Edan Diagnostics Due to Firm became...
The Issue: Firm became aware that it distributed 7 units in the U.S. that included a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Pump Recalled by CareFusion 303, Inc. Due to The syringe plunger...
The Issue: The syringe plunger grippers may fail to automatically close around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.