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. 1,095 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,095 in last 12 months

Showing 15501–15520 of 29,186 recalls

Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 11 mm x 360 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 380 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 11 mm x 420 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 11 mm x 320 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 15 mm x 360 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 9 mm x 300 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 13 mm x 340 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 340 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 440 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 11 mm x 260 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 11 mm x 400 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 125 11mm x 180mm Recalled by Zimmer Biomet, Inc....

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 130 11 mm x 400 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 280 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 11 mm x 380 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 260 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Multix MT (model number 8395415 or 8395399 or 8395381) Recalled by...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio MAX (model number 10762470) with Tube stand 3D V Recalled by Siemens...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing