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 3326133280 of 53,342 recalls

FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: WHOLE MILK CHEESE 8/6# MAGIC MOZZI Recalled by Saputo Cheese USA, Inc. Due...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA SUPREME 8/6# CONTADINO Recalled by Saputo Cheese USA, Inc. Due to...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: WHOLE MILK CHEESE 8/6# ARREZZIO CLASSIC Recalled by Saputo Cheese USA, Inc....

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# DRAGONE Recalled by Saputo Cheese...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ROSELI Recalled by Saputo Cheese...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ANTONIO Pasteurized Milk Recalled by...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Saputo Cheese USA, Inc.

Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ARREZZIO IMPERIAL Recalled by Saputo...

The Issue: Firm received one complaint from a food service customer stating a...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2016· To Your Heart's Content

Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...

The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2016· Les Emballages Knowlton Inc.

Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...

The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.

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

Class III — Low RiskOngoing
Refund
DrugNovember 22, 2016· Pfizer Inc.

Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....

The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 22, 2016· Interventional Spine Inc

Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...

The Issue: During implantation, the proximal end of the device could separate if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Scope Power Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...

The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Perspective Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Zeus-P Lumbar Interbody Device Recalled by Amendia, Inc Due to Labeling...

The Issue: Labeling error where three boxes in inventory had conflicting patient and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Scope Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...

The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing