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. 2,518 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,518 in last 12 months

Showing 2084120860 of 52,120 recalls

FoodNovember 5, 2019· Russ Davis Wholesale, Inc.

Recalled Item: Retail: Veggie Tray with Ranch Recalled by Russ Davis Wholesale, Inc. Due to...

The Issue: Products are being recalled because they may have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Avanos Medical, Inc.

Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...

The Issue: Avanos Medical has received reports stating that the central lumen of some 5...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· King Systems Corp. dba Ambu, Inc.

Recalled Item: King Vision Video Adapter Size 1/2. Laryngoscope used to examine Recalled by...

The Issue: Exhibiting a reversed image. Although the image may appear normal, the users...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 5, 2019· Dako Denmark A/S

Recalled Item: Dako Autostainer instruments: Autostainer Link 48 Recalled by Dako Denmark...

The Issue: The Autostainer instrument may not have a syringe tray installed which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Healix Knotless ADV BR 5.5 Suture Anchor Recalled by DePuy Mitek, Inc., a...

The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Medacta Usa Inc

Recalled Item: Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS Recalled by Medacta...

The Issue: Certain lot numbers of the Medacta Humeral Anatomical Cementless Metaphysis...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Trilliant Surgical, LLC

Recalled Item: 8mm HTR Sterile Hammer Toe Reaming Kit Recalled by Trilliant Surgical, LLC...

The Issue: The firm has identified that parts from the kit, lot: TSL007202, have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Immuno-Mycologics, Inc

Recalled Item: Histoplasma Immunodiffusion (ID) Antigen Recalled by Immuno-Mycologics, Inc...

The Issue: False positive results due to potential contamination of reagent.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Integra Lifesciences Sales Llc

Recalled Item: Ascension¿ Silicone PIP-Silicone PIP Sz 1 Recalled by Integra Lifesciences...

The Issue: Silicone PIP Implant mislabeled as a size 1 implant on the outer packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Healix Knotless ADV BR 4.75 Suture Anchor Recalled by DePuy Mitek, Inc., a...

The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Shimadzu Medical Systems

Recalled Item: Trinias DAP Meter Recalled by Shimadzu Medical Systems Due to The DAP meters...

The Issue: The DAP meters were found to be outside of tolerance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to the...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing