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.

55,304 total recalls
2,733 in last 12 months

Showing 2820128220 of 55,304 recalls

Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Extra Thick Black Articulating Reload with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45mm Curved Tip Articulating Vascular/Medium Reload with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMay 21, 2018· Desly International Corp.

Recalled Item: Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic Recalled by...

The Issue: Products contain undeclared peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 21, 2018· Desly International Corp.

Recalled Item: Melanie Mini Cookies with Caramel Flavor in a 17.6 oz Recalled by Desly...

The Issue: Products contain undeclared peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...

The Issue: The block used to connect the patient pallet to the couch may be assembled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMay 18, 2018· Morski Brands Inc. dba Dawn's Fresh Foods

Recalled Item: Finest Traditions Deluxe Potato Salad Recalled by Morski Brands Inc. dba...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2018· Morski Brands Inc. dba Dawn's Fresh Foods

Recalled Item: Sully's Potato Salad Recalled by Morski Brands Inc. dba Dawn's Fresh Foods...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2018· Morski Brands Inc. dba Dawn's Fresh Foods

Recalled Item: Terry's Potato Salad Recalled by Morski Brands Inc. dba Dawn's Fresh Foods...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund