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. 1,907 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
1,907 in last 12 months

Showing 1034110360 of 27,899 recalls

Medical DeviceDecember 18, 2020· Alung Technologies Inc

Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...

The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...

The Issue: Misleading error messages and a gap in the Operator Manual which affects...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Laerdal Medical (Suzhou) Co., Ltd.

Recalled Item: Laerdal Compact Suction Unit (LCSU 4) Recalled by Laerdal Medical (Suzhou)...

The Issue: Component failures may cause the unit to lose all suction. Users will need...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Hill-Rom, Inc.

Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...

The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2020· Smith & Nephew, Inc.

Recalled Item: VERSABOND AB 40 GRAMS FORMULATION 2 Recalled by Smith & Nephew, Inc. Due to...

The Issue: Potential heat and humidity exposure. The affected lot contained an atypical...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Bioventus, LLC

Recalled Item: EXOGEN Ultrasound Coupling Gel Recalled by Bioventus, LLC Due to Product may...

The Issue: Product may contain white particulates that are microbial in nature.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: A calculator/data processing module for clinical use is an electronic...

The Issue: A software error results in the unintentional removal of the serum-indices...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid...

The Issue: Bottles Missing Product Label

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...

The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...

The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Philips Ultrasound Inc

Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...

The Issue: The manufacturer discovered an issue associated with the EPIQ Image Boost...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Cook Medical Llc

Recalled Item: Disposable Humidification Flask Recalled by Cook Medical Llc Due to A small...

The Issue: A small percentage of the Disposable Humidification Flasks may have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Microbiologics Inc

Recalled Item: KWIK-STI(TM) Recalled by Microbiologics Inc Due to The expiration date on...

The Issue: The expiration date on the label of one component (negative control 0243U)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2020· Smiths Medical ASD Inc.

Recalled Item: PORTEX Bivona Cuffless Neonatal/Pediatric FlexTend Tracheostomy Tube...

The Issue: A specific model and lot number of Bivona Cuffless FlexTend Tracheostomy...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· DePuy Orthopaedics, Inc.

Recalled Item: Pinnacle Cups Recalled by DePuy Orthopaedics, Inc. Due to Certain Pinnacle...

The Issue: Certain Pinnacle Cup devices may potentially exhibit an oversized "minor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products TP Slides- IVD measure total protein (TP) Recalled...

The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) Recalled by...

The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...

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

Class II — Potential Health HazardOngoing