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 15411560 of 30,032 recalls

Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: GEN LAPAROSCOPY PACK. Medical convenience kit. Recalled by AVID Medical,...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: LAPAROSCOPY PACK. Medical convenience kit. Recalled by AVID Medical, Inc....

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: MAJOR THORACOSCOPY BASIN. Medical convenience kit. Recalled by AVID Medical,...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: PARTIAL NEPHRECTOMY PACK. Medical convenience kit. Recalled by AVID Medical,...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: CARDIAC ROBOT PACK. Medical convenience kit. Recalled by AVID Medical, Inc....

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: DAVINCI UROLOGY. Medical convenience kit. Recalled by AVID Medical, Inc. Due...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: GS ENDOSCOPY PACK. Medical convenience kit. Recalled by AVID Medical, Inc....

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: CT DAVINCI. Medical convenience kit. Recalled by AVID Medical, Inc. Due to...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: DA VINCI PACK URO/PROSTATE. Medical convenience kit. Recalled by AVID...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· FUJIFILM Healthcare Americas Corporation

Recalled Item: ASPRIRE Cristalle Mammography System (cleared under K212873) installed with...

The Issue: Devices had an unapproved slabbing software function enabled for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV....

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray Recalled by...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· RECORDATI RARE DISEASES INC.

Recalled Item: Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 Recalled by...

The Issue: Out of specification stability test result for the Caphosol B solution from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: SM_40HF_B_D_VIR3 Recalled by SEDECAL SA Due to Sedecal sent an email to its...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: SM_40HF_BDC3 Recalled by SEDECAL SA Due to Sedecal sent an email to its...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: Model Number SM-20HF-Batt Recalled by SEDECAL SA Due to Sedecal sent an...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: SM_40HF_BDC Recalled by SEDECAL SA Due to Sedecal sent an email to its...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing