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. 1,035 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,035 in last 12 months

Showing 22781–22800 of 53,342 recalls

Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Dual-Sided Interhemispheric Recalled by Ad-Tech Medical Instrument...

The Issue: Supplemental information provided with devices indicates that the subdural...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...

The Issue: Supplemental information provided with devices may indicate that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Howmedica Osteonics Corp.

Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...

The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: Battery short-run times and unanticipated stoppage may be due to user not...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...

The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci Surgical System Recalled by Intuitive Surgical, Inc. Due to One da...

The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2019· Bausch & Lomb

Recalled Item: Lotemax (loteprednol etabonate ophthalmic gel 0.5%) Recalled by Bausch &...

The Issue: Failed Stability Specifications: Out of specification for viscosity.

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

Class III — Low RiskOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 14, 2019· Stanley Security Solutions Inc

Recalled Item: STANLEY Healthcare Arial 54315 Network Manager Recalled by Stanley Security...

The Issue: STANLEY Healthcare has received reports of outages on the Arial nurse call...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2019· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Capiox NX19 Oxygenator (East Orientation) Recalled by Terumo...

The Issue: Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2019· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Capiox NX19 Oxygenator With Reservoir (West Orientation) P/N:...

The Issue: Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2019· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Capiox NX19 Oxygenator With Reservoir (East Orientation) P/N:...

The Issue: Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor...

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

Class II — Potential Health HazardOngoing