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. 2,420 recalls have been distributed to New Hampshire in the last 12 months.
Showing 18361–18380 of 27,899 recalls
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raindrop Near Vision Inlay Recalled by Revision Optics Inc Due to ReVision...
The Issue: ReVision Optics has updated the instructions for use (IFU) for the Raindrop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF#...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Table Patient Step on RFX/SFX Recalled by GE Healthcare, LLC Due to Reported...
The Issue: Reported incidents of a patient step detaching from the table. A fall from a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORFLO Recalled by CORPAK MedSystems, Inc. Due to Firm is initiating...
The Issue: Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORFLO Recalled by CORPAK MedSystems, Inc. Due to Firm is initiating...
The Issue: Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORFLO PEG Kit Recalled by CORPAK MedSystems, Inc. Due to Firm is initiating...
The Issue: Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...
The Issue: The stopcock was found to have punctures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XPT System Software Versions V1.0.1 Recalled by Siemens...
The Issue: Multiple software issues, which may affect the operation and workflow of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.