Product Recalls in New Hampshire

Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,534 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,534 in last 12 months

Showing 1044110460 of 27,899 recalls

Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Biomet, Inc.

Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...

The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...

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

Class II — Potential Health HazardOngoing
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