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 2424124260 of 53,342 recalls

DrugJanuary 29, 2019· US Compounding Inc

Recalled Item: Ephedrine Sulfate Recalled by US Compounding Inc Due to Lack of assurance of...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2019· COLLINS AEROSPACE

Recalled Item: TASE 400 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...

The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2019· COLLINS AEROSPACE

Recalled Item: TASE 500 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...

The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Lupin Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications: OOS results observed in any...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX2 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX3 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX3 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX2 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Spacelabs Healthcare, Inc.

Recalled Item: Spacelabs Healthcare Smart Disclosure System Recalled by Spacelabs...

The Issue: Several reports were received that patient records were printed with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Applied Medical Resources Corp

Recalled Item: Kii Fios First Entry Recalled by Applied Medical Resources Corp Due to The...

The Issue: The product may not have met sterility requirements . Use of a non-sterile...

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

Class II — Potential Health HazardOngoing
DrugJanuary 25, 2019· Akorn Inc

Recalled Item: Clobetasol Propionate Emollient Cream 0.05% Recalled by Akorn Inc Due to...

The Issue: Failed Stability Specification; out of specification (OOS) results for a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 25, 2019· Philips North America, LLC

Recalled Item: Fetal Spiral Electrode Recalled by Philips North America, LLC Due to During...

The Issue: During use of the Philips FSE, it is possible for the metal electrode tip to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2019· Medrobotics Corporation

Recalled Item: Obturator (long cone) Recalled by Medrobotics Corporation Due to The weld...

The Issue: The weld may break, resulting in the rod separating from the cone of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2019· Medrobotics Corporation

Recalled Item: Obturator (shortcone) Recalled by Medrobotics Corporation Due to The weld...

The Issue: The weld may break, resulting in the rod separating from the cone of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2019· Philips North America, LLC

Recalled Item: Lithium-ion Rechargeable Batteries for the Philips MX40 Wearable Monitor by...

The Issue: Lithium-ion Rechargeable Batteries for the Philips MX4O Wearable Monitor may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2019· Agfa N.V.

Recalled Item: PET Plates Coated Film-MONOMEDBV2S2- Radiographic Film Recalled by Agfa N.V....

The Issue: Due to an inhomogeneous coating solution, pinholes can become visible in...

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

Class III — Low RiskOngoing
DrugJanuary 24, 2019· US Compounding Inc

Recalled Item: LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%)...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Labels are missing lot...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: BromSite (bromfenac ophthalmic solution) 0.075% Recalled by Sun...

The Issue: Bromfenac Ophthalmic Solution, 0.075% (Sterile 5 mL) may have a lack of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 24, 2019· Maquet Cardiovascular, LLC

Recalled Item: AXIUS Blower Mister Product Code/: CB-1000 The Axius Blower Recalled by...

The Issue: Potential lack of carbon dioxide (CO2) flow that may result in a procedural...

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

Class II — Potential Health HazardOngoing
FoodJanuary 23, 2019· THRIVE MARKET

Recalled Item: Thrive Market Organic Coconut Butter 16 oz. SKU/Recalled by THRIVE MARKET...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund