Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,520 in last 12 months

Showing 2964129660 of 53,342 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 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 4, 2017· ZOLL Medical Corporation

Recalled Item: OneStep CPR Complete Recalled by ZOLL Medical Corporation Due to A portion...

The Issue: A portion of one lot of ZOLL OneStep Complete Electrodes for adults will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2017· Gyrus ACMI, Inc.

Recalled Item: Gyrus ACMI Round Cutting Burrs - to be used with the Diego Elite system...

The Issue: "Chattering" when cutting burrs are used in bone.

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· 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
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 2, 2017· Teva Pharmaceuticals USA

Recalled Item: Glipizide Extended-Release Tablets (anti-diabetic agent) Recalled by Teva...

The Issue: Failed Moisture Limits: out of specification test results for water content...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Diocto Syrup Recalled by The Harvard Drug Group Due to Microbial...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

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

Recalled Item: Rugby Diocto Liquid Recalled by The Harvard Drug Group Due to Microbial...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

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

Recalled Item: Rugby Aller-chlor (Chlorpheniramine Maleate Syrup Recalled by The Harvard...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

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

Recalled Item: Major Senna Syrup Natural Vegetable Laxative Recalled by The Harvard Drug...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

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

Recalled Item: Rugby Senexon Liquid Natural Vegetable Stimulant Recalled by The Harvard...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

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

Recalled Item: Amrita Mango Coconut Energy 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