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. 2,727 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,727 in last 12 months

Showing 1984119860 of 29,093 recalls

Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Zimmer Biomet, Inc.

Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...

The Issue: Complaints have been reported that the handpiece is inoperable. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: V6 Rear Case Assembly Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: 4 PORT "OFF" MANIFOLD Recalled by ICU Medical, Inc. Due to ICU Medical Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner and Reprocessor System 208V Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSDUCER KIT FOR MEDICAL CTR. AT BOWLING GREEN Recalled by ICU Medical,...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Monitoring Kit #3 w/03 ml Flush Device for Childrens Hosp Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV MONITORING KIT Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Cath Lab Kit w/Waste Bag System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV MONITORING KIT WITH SAFESET" RESERVOIR AND BLOOD SAMPLING PORT...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV MONITORING KIT Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: PERFUSION KIT FOR UNIV. OF IOWA Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing