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. 2,439 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,439 in last 12 months

Showing 3980139820 of 52,120 recalls

Medical DeviceMay 4, 2015· Smiths Medical Asd Inc

Recalled Item: Low Volume Extension Set Recalled by Smiths Medical Asd Inc Due to Smiths...

The Issue: Smiths Medical has become aware of an issue with the Low Volume Extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2015· Remel Inc

Recalled Item: Remel Blood Agar (TSA w/sheep blood) plate packaged Recalled by Remel Inc...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2015· Synovis Surgical Innovations, Inc.

Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...

The Issue: Baxter healthcare is recalling specific product codes of Vascu-Guard...

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

Class I — Serious Health HazardOngoing
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Sun Rich Apple Slices with Caramel Dip Recalled by Sun Rich Fresh Foods Inc...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Sunshine Salad Kit Recalled by Sun Rich Fresh Foods Inc Due to Potential...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Fresh Cut Red Apple Slices 2 x 3 lbs Recalled by Sun Rich Fresh Foods Inc...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Sub Way Apple Slices Recalled by Sun Rich Fresh Foods Inc Due to Potential...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Fresh Cut Mixed Apple slices Recalled by Sun Rich Fresh Foods Inc Due to...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Top Taste, Inc

Recalled Item: Fetting's Jumbo 2.5 oz Cinnamon Roll Dough 140 Recalled by Top Taste, Inc...

The Issue: Firm discovered than an incorrect ingredient label which did not state...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 1, 2015· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...

The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Biomet, Inc.

Recalled Item: Unilateral external fixation ankle clamp Product Usage: Unilateral external...

The Issue: Ankle clamp was assembled incorrectly; the offset of the pin to the pivot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: Base for Terumo Advanced Perfusion System 1 Recalled by Terumo...

The Issue: Terumo CVS is implementing field correction activities to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo CVS is implementing field correction activities to address the...

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

Class II — Potential Health HazardOngoing
DrugApril 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit Recalled by Mission...

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund