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. 2,508 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,508 in last 12 months

Showing 1180111820 of 27,899 recalls

Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: Philips Zenition 50 Recalled by Philips North America, LLC Due to When...

The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: HeartStart MRx Processor Board PCA Replacement Kits 453563478461 Recalled by...

The Issue: Damaged ESD bags used for storing components in Processor PCA Replacement Kits

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: Philips Zenition 70 Recalled by Philips North America, LLC Due to When...

The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2020· BD SWITZERLAND SARL

Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...

The Issue: The products have the potential to leak between the connection of the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2020· CooperSurgical, Inc.

Recalled Item: CooperSurgical Dilator/Sound Set Recalled by CooperSurgical, Inc. Due to The...

The Issue: The seal of the sterile pouch may be compromised on one lot of the Milex...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2020· BD SWITZERLAND SARL

Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...

The Issue: The products have the potential to leak between the connection of the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2020· BD SWITZERLAND SARL

Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...

The Issue: The products have the potential to leak between the connection of the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2020· Wright Medical Technology Inc

Recalled Item: WRIGHT INBONE Tibial Tray Recalled by Wright Medical Technology Inc Due to...

The Issue: One lot of INBONE Tibial Trays is missing the plasma coating.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2020· The Binding Site Group, Ltd.

Recalled Item: The Optilite Clinical Chemistry Analyzer. IVD. Model Number: IE700....

The Issue: A software issue that may affect the analyzer's result accuracy.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2020· Qiagen Sciences LLC

Recalled Item: therascreen EGFR RGQ PCR Kit (24) Recalled by Qiagen Sciences LLC Due to...

The Issue: There is a risk for a false mutation positive result in rare cases resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2020· Argon Medical Devices, Inc

Recalled Item: PAC Tray/5 Catheter Introducer Tray 8F Recalled by Argon Medical Devices,...

The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2020· Argon Medical Devices, Inc

Recalled Item: Arterial Line Kit 20ga X 3" Recalled by Argon Medical Devices, Inc Due to...

The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2020· Argon Medical Devices, Inc

Recalled Item: Arterial Line Kit 20ga X 3" Recalled by Argon Medical Devices, Inc Due to...

The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Inpeco S.A.

Recalled Item: Accelerator a3600 Automation System using the Aliquoter Module (Inpeco P/N...

The Issue: In certain firmware versions, in case a Clot Detection error (error code...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Inpeco S.A.

Recalled Item: Abbott Accelerator a3600 Recalled by Inpeco S.A. Due to When analyzer sample...

The Issue: When analyzer sample carousel lid remains open or manual process is too...

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

Class II — Potential Health HazardOngoing