Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,820 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,820 in last 12 months

Showing 1098111000 of 30,153 recalls

Medical DeviceNovember 30, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno Recalled by Siemens Medical...

The Issue: When the user changes frame rates from lower frequency (e.g. 10 f/s) to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: 3.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific lots...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Comprehensive Total Shoulder System/Bio-Modular Choice Shoulder System...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Oxford Fixed Lateral Recalled by Biomet, Inc. Due to Specific lots of...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Custom Cancellous Thread Recalled by Biomet, Inc. Due to Specific lots of...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Sterile Trac System Thinflap 24 MM Burr Hole Plate Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: PHOENIX Recalled by Biomet, Inc. Due to Specific lots of multiple sterile...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: M/H MODULAR STEM Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: OSS Polyethylene Tibial Bushing Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RINGLOC BIPOLAR Hip System Bi Polar Locking Ring Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder System Recalled by Biomet, Inc. Due to...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: 4.0/5.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RINGLOC ACETABULAR SYSTEM Self-tapping bone screws Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: 6.5/8.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Titanium IFS Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RingLoc+ Quick Connect Drill Bit Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RapidFire Clip Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to System...

The Issue: System does not trigger a cancel command followed by a reload of the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing