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. 2,348 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,348 in last 12 months

Showing 3250132520 of 49,311 recalls

Medical DeviceJune 24, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...

The Issue: A variation in flute depth on the routers was observed. The variation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

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

Class I — Serious Health HazardOngoing
DrugJune 24, 2016· Teva North America

Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva North America Due to...

The Issue: Superpotent drug: Out of specification test result for assay during...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2016· Hospira Inc.

Recalled Item: Diazepam Injection USP 10mg/2mL (5 mg/mL Recalled by Hospira Inc. Due to...

The Issue: Crystallization: Product contains particulate identified to be crystallized...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 23, 2016· Inner Health Group, Inc dba Michael's Naturopathic Programs

Recalled Item: Michael's Naturopathic Programs Cholesterol Metabolism Factors 270 count...

The Issue: May contain undeclared milk (in the form of calcium caseinate) and soy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJune 23, 2016· Mondelez International

Recalled Item: Nabisco Honey Maid Teddy Grahams Cinnamon Cubs Graham Snacks Net Recalled by...

The Issue: Teddy Graham Cub Snacks were produced using Grain Craft Flour containing...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 23, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...

The Issue: Incorrect values for the volume calculation. Software update VB30B via...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Modular Handle Triathlon Instruments Recalled by...

The Issue: Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Olympus Corporation of the Americas

Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...

The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with...

The Issue: It was reported that the secondary locking mechanism, and its corresponding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Edan Diagnostics

Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...

The Issue: Incorrect CO2 readings with some patient monitors.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...

The Issue: Varian Medical Systems has received reports that unintended changes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...

The Issue: Varian Medical Systems has received reports that unintended changes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...

The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: Anastoclip AC 8cm 35 Clips (1 Each} Medium REF # Recalled by LeMaitre...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: Anasto AC Closure System and Anasto Universal Clip Remover- Anasto Recalled...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# e4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Sorin Group USA, Inc.

Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...

The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# e4001-00 The Anastoclip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing