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 3714137160 of 52,120 recalls

FoodDecember 9, 2015· Nestle Waters North America

Recalled Item: Sweet Leaf Organic Raspberry Iced Tea Recalled by Nestle Waters North...

The Issue: Product contains glass particles

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2015· Nestle Waters North America

Recalled Item: Sweet Leaf Organic Original Sweet Tea Recalled by Nestle Waters North...

The Issue: Product contains glass particles

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2015· Nestle Waters North America

Recalled Item: Sweet Leaf Organic Half and Half Lemonade Tea Recalled by Nestle Waters...

The Issue: Product contains glass particles

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2015· Nestle Waters North America

Recalled Item: Sweet Leaf All Natural Citrus Green Tea Recalled by Nestle Waters North...

The Issue: Product contains glass particles

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2015· Nestle Waters North America

Recalled Item: Sweet Leaf Organic Tea Mint & Honey Recalled by Nestle Waters North America...

The Issue: Product contains glass particles

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2015· Nestle Waters North America

Recalled Item: Sweet Leaf All Natural Peach Iced Tea Recalled by Nestle Waters North...

The Issue: Product contains glass particles

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 9, 2015· Zimmer Biomet, Inc.

Recalled Item: Zimmer Universal Locking System 3.5mm Locking Reconstruction Plate Straight...

The Issue: The product on the package label did not match what was inside the package....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...

The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing