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. 2,385 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,385 in last 12 months

Showing 2210122120 of 27,899 recalls

Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Hysto Pack Recalled by Covidien LLC Due to Devon Light Gloves contain splits...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the cable cart and the corrugated hose are unable to move freely, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Halyard Health, Inc

Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to Study...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· CooperSurgical, Inc.

Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...

The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Alphatec Spine, Inc.

Recalled Item: 4.0mm Variable Angle Recalled by Alphatec Spine, Inc. Due to Mislabeling

The Issue: During a field audit it was discovered by an employee that a 16mm Trestle...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Philips Ultrasound, Inc.

Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...

The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Philips Ultrasound, Inc.

Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...

The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· BTE Technologies, Inc.

Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...

The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Bard Peripheral Vascular Inc

Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...

The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Synthes, Inc.

Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...

The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Spinal Elements, Inc

Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...

The Issue: Some rods may not meet the appropriate traceability requirements including...

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

Class III — Low RiskOngoing