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. 2,563 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,563 in last 12 months

Showing 2502125040 of 53,342 recalls

DrugOctober 15, 2018· Zero Xtreme USA

Recalled Item: Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro...

The Issue: Marketed Without an Approved NDA/ANDA: Undeclared Sibutramine

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2018· Smiths Medical ASD Inc.

Recalled Item: Medfusion¿ Model 4000 Syringe Infusion Pump Recalled by Smiths Medical ASD...

The Issue: Customers who utilize PharmGuard¿ Server Software (PGS) with Medfusion¿ 4000...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Compress Devices and Instruments: Item Number/Item Description 178350...

The Issue: Correction to update the surgical technique for the Compress System. To make...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...

The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Atrium Medical Corporation

Recalled Item: Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE Recalled by Atrium Medical...

The Issue: This recall has been initiated in response to a seal defect found in certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...

The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· St. Jude Medical, Inc.

Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....

The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...

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

Class II — Potential Health HazardOngoing
DrugOctober 11, 2018· Lannett Company, Inc.

Recalled Item: HydrOXYzine HYDROCHLORIDE SYRUP (HydrOXYzine Hydrochloride Oral Solution...

The Issue: CGMP Deviations: cleaning procedures during manufacturing caused out of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...

The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...

The Issue: It was identified that the volume of air inside the mattress may expand in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2018· Synaptive Medical Inc

Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...

The Issue: This recall has been initiated due to a software defect found in the Guide...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 9, 2018· Theragenics Corporation

Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...

The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
FoodOctober 9, 2018· World Variety Produce Inc.

Recalled Item: Melissa's Hatch Chile Clean Snax Recalled by World Variety Produce Inc. Due...

The Issue: Firm discovered that Hatch Chile Clean Snax lists peanuts in the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: ImmunoBooster Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Cold + Flu Relief Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund