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. 2,458 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,458 in last 12 months

Showing 3462134640 of 52,120 recalls

Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Stanley Security Solutions Inc

Recalled Item: Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is...

The Issue: Devices were incorrectly programmed during manufacturing therefore...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Draeger Medical, Inc.

Recalled Item: Babytherm 8004/8010 Recalled by Draeger Medical, Inc. Due to Risk associated...

The Issue: Risk associated with operating the device in skin temperature mode with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Olympus Scientific Solutions Americas

Recalled Item: Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical...

The Issue: Trigger lock option does not always prevent x-ray generation. Specifically...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Dynasty Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· Omega Medical Imaging, Inc.

Recalled Item: 2 over 2 Elevating Monitor Suspension - Omega Medical Imaging Recalled by...

The Issue: Elevating Monitor Suspension separated from the lifting column bracket

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 20, 2016· Karl Storz Endoscopy

Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...

The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2016· Medtronic Navigation

Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...

The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2016· W & C dba The Apothecary

Recalled Item: Calcium Gluconate 2.5% -- 20 mL PLASTIC SYRINGE Recalled by W & C dba The...

The Issue: Lack of assurance of sterility: This recall includes of all unexpired lots...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2016· W & C dba The Apothecary

Recalled Item: Prostaglandin 200 mcg/ 0.1 mL -- 25 mL GLASS VIAL Recalled by W & C dba The...

The Issue: Lack of assurance of sterility: This recall includes of all unexpired lots...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2016· W & C dba The Apothecary

Recalled Item: Papaverine 75 mg / Phentolamine 2.5 mg / Prostaglandin 25 Recalled by W & C...

The Issue: Lack of assurance of sterility: This recall includes of all unexpired lots...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2016· W & C dba The Apothecary

Recalled Item: Papaverine 30 mg / Phentolamine 1 mg / mL -- 5 mL GLASS VIAL Recalled by W &...

The Issue: Lack of assurance of sterility: This recall includes of all unexpired lots...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2016· W & C dba The Apothecary

Recalled Item: Calcium Gluconate 1% -- 1000 mL VIAFLEX IV BAG Recalled by W & C dba The...

The Issue: Lack of assurance of sterility: This recall includes of all unexpired lots...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund