Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,666 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,666 in last 12 months

Showing 55215540 of 29,186 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· 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· Instrumentation Laboratory

Recalled Item: GEM Premier 3000 PAK - pH Recalled by Instrumentation Laboratory Due to...

The Issue: Internal testing identified that the GEM Premier PAKs (cartridges) may...

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· Instrumentation Laboratory

Recalled Item: GEM Premier 3000 PAK - pH Recalled by Instrumentation Laboratory Due to...

The Issue: Internal testing identified that the GEM Premier PAKs (cartridges) may...

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· Instrumentation Laboratory

Recalled Item: GEM Premier 3000 PAK - pH Recalled by Instrumentation Laboratory Due to...

The Issue: Internal testing identified that the GEM Premier PAKs (cartridges) may...

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