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 3088130900 of 53,342 recalls

FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: Topfer Lactana Bio 1 Anfangsmilch Recalled by 3CS ORGANICS LLC Due to The...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: HOLLE Bio Lait Pour Nourrissons Au Lait De Chevre Recalled by 3CS ORGANICS...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: Lebenswert Bioland Anfangsmilch1 Recalled by 3CS ORGANICS LLC Due to The...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: HIPP Tetrapack-Liquid Recalled by 3CS ORGANICS LLC Due to The product is not...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: HIPP Organic Comb Hungry Infant Milk Recalled by 3CS ORGANICS LLC Due to The...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: HIPP Anti- AR Bio-Spezialnahrung Recalled by 3CS ORGANICS LLC Due to The...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2017· X-Gen Pharmaceuticals Inc.

Recalled Item: Nystatin Topical Powder Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Presence of Foreign Substance: potential presence of plastic particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Presence of an impurity peak...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 17, 2017· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...

The Issue: Contraindication language updated in the Instructions For Use (IFU) to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2017· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...

The Issue: Contraindication language updated in the Instructions For Use (IFU) to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2017· Z-Medica, LLC

Recalled Item: QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may...

The Issue: Packaging breach may compromise sterility

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

Class II — Potential Health HazardOngoing
DrugMay 16, 2017· Lupin Limited (Unit 1)

Recalled Item: Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02...

The Issue: Contraceptive Tablets Out of Sequence- First 4 pills of the packet are...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 16, 2017· GlaxoSmithKline, LLC

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Recalled by GlaxoSmithKline, LLC...

The Issue: Defective Delivery System: Elevated number of units with out of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis Vibe Systems with Software Version VD10B Recalled by Siemens Medical...

The Issue: Software error. In Sensis Vibe systems with software version VD10B, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Beckman Coulter Inc

Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...

The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· bioMerieux, Inc.

Recalled Item: VIDAS Testosterone Recalled by bioMerieux, Inc. Due to Complaints were...

The Issue: Complaints were received from customers observing falsely overestimate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Perkinelmer Life Sciences, Inc.

Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...

The Issue: Potential for electric shock in the case of a failure to install the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...

The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...

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

Class II — Potential Health HazardOngoing
FoodMay 12, 2017· Nutri-Dyn Midwest, Inc.

Recalled Item: Nutri-Dyn Calcium D-Glucarate Plus Recalled by Nutri-Dyn Midwest, Inc. Due...

The Issue: During production of St. John's Wort, Lot 160876, a number of bottles were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 12, 2017· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211...

The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...

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

Class II — Potential Health HazardOngoing