Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,636 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,636 in last 12 months

Showing 54615480 of 28,245 recalls

Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Staar Surgical Company

Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...

The Issue: Their is a potential that intraocular implant devices may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: IRON assay Recalled by Sentinel CH SpA Due to A high recovery of Iron assay...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: Alinity c Iron Reagent Recalled by Sentinel CH SpA Due to A high recovery of...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2023· Olympus Corporation of the Americas

Recalled Item: TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP Recalled by Olympus Corporation...

The Issue: Fiberscopes do not have adequate data to support that the suction flow rate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2023· Boston Scientific Corporation

Recalled Item: EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Recalled...

The Issue: Poor image quality due to fluid ingress in the lens.

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

Class II — Potential Health HazardOngoing