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. 2,627 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,627 in last 12 months

Showing 1398114000 of 29,286 recalls

Medical DeviceMay 28, 2019· GN Otometrics

Recalled Item: The ICS CHARTR EP 200 Recalled by GN Otometrics Due to There is a risk to...

The Issue: There is a risk to the healthcare professional or patient of exposure to...

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

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

Recalled Item: SOMATOM go.Now (Model #11061620) Recalled by Siemens Medical Solutions USA,...

The Issue: The potential sporadic performance problems may result in scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Nobel Biocare Usa Llc

Recalled Item: Healing Abutment Conical Connection RP 0 3.6 x 5mm Recalled by Nobel Biocare...

The Issue: Packaged dental implant healing abutments were found to contain the wrong...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT: 1) Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) CF 6.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) HVT 6.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Preformed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Uncuffed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS Recalled by Teleflex Medical Due to This voluntary...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2019· Richard Wolf Medical Instruments Corp.

Recalled Item: E-Line Cutting Electrode 11.5Fr Mono 0 degrees Recalled by Richard Wolf...

The Issue: E-Line Cutting Electrode package 8416.0305 contains E-Line Hook Electrode...

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

Class II — Potential Health HazardOngoing