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. 2,478 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,478 in last 12 months

Showing 2926129280 of 52,120 recalls

Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2017· OrthoPediatrics Corp

Recalled Item: Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Recalled by...

The Issue: The 7mm diameter uniaxial pedicle screws have been color anodized with the...

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

Class II — Potential Health HazardOngoing
DrugAugust 3, 2017· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Lorazepam Oral Concentrate Recalled by Amneal Pharmaceuticals of New York,...

The Issue: Defective Delivery System: the dropper measurement markings may be reversed,...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 3, 2017· MEDLINE INDUSTRIES INC

Recalled Item: Vitamin A&D Ointment (petroleum 93.5%) Recalled by MEDLINE INDUSTRIES INC...

The Issue: Labeling Mixup; the individual A&D ointment foil packets are incorrectly...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2017· KVK-Tech, Inc.

Recalled Item: Phentermine HCL Capsules Recalled by KVK-Tech, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...

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

Class III — Low RiskOngoing
Refund
FoodAugust 3, 2017· Go Fresh

Recalled Item: Broccoli Florets packaged with the following [Product Brand Recalled by Go...

The Issue: Broccoli has the potential to be contaminated with E. coli O26

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2017· Go Fresh

Recalled Item: US Foods VEG MIX BROC/RED-ON-PEP STRIP Recalled by Go Fresh Due to Potential...

The Issue: Broccoli has the potential to be contaminated with E. coli O26

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2017· Go Fresh

Recalled Item: Imperial Fresh Veg Blend 7-Way Recalled by Go Fresh Due to Potential E. coli...

The Issue: Broccoli has the potential to be contaminated with E. coli O26

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· Amrita Health Foods

Recalled Item: Amrita Dark Chocolate Quinoa 15g Protein Bar Recalled by Amrita Health Foods...

The Issue: Product may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 2, 2017· Amrita Health Foods

Recalled Item: Amrita Apricot Strawberry Protein Bar Recalled by Amrita Health Foods Due to...

The Issue: Product may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 2, 2017· Amrita Health Foods

Recalled Item: Amrita Sunflower Butter & Jelly 15g Protein Bar Recalled by Amrita Health...

The Issue: Product may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 2, 2017· Perkinelmer Life Sciences, Inc.

Recalled Item: JANUS & JANUS G3 Automated Workstation is an automated programmable Recalled...

The Issue: We have become aware through internal testing that JANUS and Janus G3...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2017· Instrumentation Laboratory Co.

Recalled Item: Hemosll ReadiPlasTin (20 ml Size) Recalled by Instrumentation Laboratory Co....

The Issue: Instrumentation Laboratory Co. received customer reports of performance...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2017· OriGen Biomedical, Inc.

Recalled Item: The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel Recalled by...

The Issue: Two users have reported to OriGen that a VV28F OriGen Reinforced Dual Lumen...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 2, 2017· Haemonetics Corporation

Recalled Item: Cell Saver Elite Processing Kit Recalled by Haemonetics Corporation Due to...

The Issue: Haemonetics has received isolated reports that in some cases the 70ml...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2017· Haemonetics Corporation

Recalled Item: Cell Saver 5/5+ Bowl Set Recalled by Haemonetics Corporation Due to...

The Issue: Haemonetics has received isolated reports that in some cases the 70ml...

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

Class II — Potential Health HazardOngoing
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Polyvitamin Liquid with Iron Recalled by The Harvard Drug Group Due to...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Leader Liquid Multivitamin Supplement for Infants and Toddlers Recalled by...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Fer-iron Liquid Recalled by The Harvard Drug Group Due to The...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Major Poly-Vita Drops Recalled by The Harvard Drug Group Due to The...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund