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. 2,532 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,532 in last 12 months

Showing 2734127360 of 53,342 recalls

Medical DeviceMay 2, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...

The Issue: The bottles are mislabeled with an incorrect part number.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Roche Molecular Systems, Inc.

Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...

The Issue: Cross-contamination of samples has been reported when running the existing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Heartware

Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...

The Issue: Possible transient electrical connection interruption between an HVAD System...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 2, 2018· Smith & Nephew, Inc.

Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...

The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...

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

Class II — Potential Health HazardOngoing
DrugMay 1, 2018· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2018· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2018· AuroMedics Pharma LLC

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by AuroMedics Pharma LLC...

The Issue: Presence of Particulate Matter: confirmed customer report for presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 1, 2018· AuroMedics Pharma LLC

Recalled Item: Ampicillin and Sulbactam for Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Presence of Particulate Matter: confirmed customer report of the presence of...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2018· Bob's Red Mill Natural Foods, Inc.

Recalled Item: Bob's Red Mill 100% Whole Wheat Bread Mix Recalled by Bob's Red Mill Natural...

The Issue: 100% Whole Wheat Bread Mix is recalled due to undeclared wheat in the label...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zeego Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno Interventional Fluoroscopic X-Ray System Recalled by Siemens...

The Issue: If the C-arm is manually moved in the longitudinal direction to a fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost Classic X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing