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. 2,480 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,480 in last 12 months

Showing 3970139720 of 53,342 recalls

Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Precision RXi 23A/32A Analog System Recalled by GE Healthcare...

The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE RP CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE RP PS ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED Recalled by DePuy Orthopaedics,...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Precision RXi Digital system Recalled by GE Healthcare Due to...

The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV RP PS TB TRL SZ10 INTENDED USE: The Recalled by DePuy...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV RP CR ARTICULATION SURFACE SZ1 Recalled by DePuy Orthopaedics,...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE CONV FB CR ARTICULATION SURFACE SZ1 INTENDED USE: The Recalled by...

The Issue: Potential for the Balseal, a small wire spring coil located on the post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A reported incident of a...

The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and...

The Issue: The SFD/IDD safety mechanism may not engage properly at the lower range of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2015· BioMerieux SA

Recalled Item: Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro...

The Issue: QC results were out of range resulting in false resistant strains.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Abbott Laboratories

Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...

The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Justright Surgical, LLC

Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...

The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Justright Surgical, LLC

Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...

The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...

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

Class II — Potential Health HazardOngoing
DrugJune 10, 2015· The Harvard Drug Group, LLC

Recalled Item: OXYCODONE HCl C-II Tablets Recalled by The Harvard Drug Group, LLC Due to...

The Issue: Superpotent Drug: Confirmed customer complaint of a single unit dose blister...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2015· AstraZeneca Pharmaceuticals LP

Recalled Item: NEXIUM¿ (esomeprazole magnesium) Recalled by AstraZeneca Pharmaceuticals LP...

The Issue: Presence of Foreign Tablets/Capsules: Confimed customer compliant by a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 10, 2015· Dr. Pepper Snapple Group Inc

Recalled Item: Diet Bubba Cola Recalled by Dr. Pepper Snapple Group Inc Due to The firm was...

The Issue: The firm was notified by one of it's retail stores that the ingredient...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 10, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...

The Issue: There is a potential issue that could result to collision between the C-arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2015· Northern Digital Inc.

Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...

The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2015· Synthes (USA) Products LLC

Recalled Item: Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA)...

The Issue: The height of one of the three guiding pins of the Helical Blade Inserter...

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

Class II — Potential Health HazardOngoing