Product Recalls in Maryland

Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,774 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,774 in last 12 months

Showing 1840118420 of 29,093 recalls

Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU Recalled by...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD Recalled by...

The Issue: Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2017· Hitachi Medical Systems America Inc

Recalled Item: Arietta 70 Ultrasound System Intended for use by trained personnel (doctor...

The Issue: The strength of the arm mounting mechanism was insufficient and had to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2017· GE Healthcare, LLC

Recalled Item: Carestation 620 A1 Recalled by GE Healthcare, LLC Due to Carestation 620,...

The Issue: Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Skewers Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: LapSac Introducer Set Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Circadiance LLC

Recalled Item: SmartMonitor 2 PS/PSL Recalled by Circadiance LLC Due to Circadiance has...

The Issue: Circadiance has determined that it is possible for certain Smart Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Reapproximator Plate Recalled by Cook Inc. Due to COOK Medical...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 Recalled by Toshiba...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: LapSac Introducer Recalled by Cook Inc. Due to COOK Medical is initiating a...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Reapproximator Set Recalled by Cook Inc. Due to COOK Medical...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: APLIO 500 TUS-A500 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: XARIO 200 TUS-X200 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Endoscopic Curved Needle Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: XARIO 100 TUS-X100 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: APLIO 300 TUS-A300 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: FEM IM NAIL 15MMDX30CM Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSA-FX II STD TUBE 130DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing