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. 2,959 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,959 in last 12 months

Showing 12811300 of 55,304 recalls

Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Magnetic Rings for SAFE-T-FILL Blood Gas Capillaries Recalled by...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Collection Tube Extender Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: AFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: B105P Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: CARESCAPE ONE Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: Portrait VSM Model nos. 6660000-666 Monitor Recalled by GE Healthcare...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: Carescape B450 Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator 11mm. Cranial Perforator. Recalled by Integra...

The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene...

The Issue: Zimmer Biomet is conducting a medical device recall for two (2) lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene...

The Issue: Zimmer Biomet is conducting a medical device recall for two (2) lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator 9mm. Cranial Perforator. Recalled by Integra...

The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2025· Synthes (USA) Products LLC

Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...

The Issue: Although the etched length on the screw is correct, the length marked on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Synthes (USA) Products LLC

Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...

The Issue: Although the etched length on the screw is correct, the length marked on the...

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

Class II — Potential Health HazardOngoing