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. 2,367 recalls have been distributed to New Hampshire in the last 12 months.
Showing 25321–25340 of 27,899 recalls
Recalled Item: Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanta VS Grafts <6mm Intended for use in arterial vascular reconstruction...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanta SuperSoft Grafts >or= 6mm Intended for use in arterial Recalled by...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flixene IFG with Assisted Delivery Intended for use in arterial Recalled by...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanta SuperSoft Grafts <6mm Intended for use in arterial vascular Recalled...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanta VS Grafts >or= 6mm Intended for use in arterial vascular...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AperFix AM Femoral Implant Recalled by Cayenne Medical Inc. Due to Potential...
The Issue: Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acuson SC2000 volume imaging ultrasound systems at software version 3.0....
The Issue: Software issue results in inaccurate 3D image may result in ablation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A....
The Issue: TempaDot products may have been mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tray Surgical Recalled by Medtronic Xomed, Inc. Due to The firm will recall...
The Issue: The firm will recall and replace the identified instrument trays in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Tecan US-II. For use in the screening and detection Recalled by...
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Tecan US-I. For use in the screening and detection Recalled by...
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...
The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1) Asnis III Cannulated Screw 4.0x40mm TL Recalled by Stryker...
The Issue: Stryker received a report that the length of the cannulated screw asnis III,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain AG. For use in the screening and detection of cervical cancer....
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.