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. 2,932 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,932 in last 12 months

Showing 60216040 of 30,032 recalls

Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Airway Mobilescope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Tracheal Intubation Fiberscope Recalled by Olympus Corporation of...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V Recalled by Olympus...

The Issue: Recent reports of patient infection.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Airway Mobilescope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-MR1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-C1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton C1/T1/MR1 Recalled by Hamilton Medical, Inc. Due to Degrading...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Zimmer, Inc.

Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...

The Issue: The outer package labeling and product etch are for a Size 6, however, the...

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

Class II — Potential Health HazardOngoing