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 25661–25680 of 27,899 recalls
Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile...
The Issue: This is a recall expansion from the 2010 recall which now includes seven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sovereign¿ Compact Phacoemulsification System Recalled by Abbott Medical...
The Issue: Abbott Medical Optics Inc. (AMO) initiated this Urgent Notice of Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen...
The Issue: Failure to submit a premarket submission and gain approval of a medical device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen...
The Issue: Failure to submit a premarket submission and gain approval of a medical device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to leaking pouches
The Issue: leaking pouches
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...
The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...
The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...
The Issue: There is a possibility that the pump head was not shipped in the locked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....
The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...
The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Plus System The CoaguChek XS Plus system for Recalled by Roche...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Pro System The CoaguChek XS Pro System (CoaguChek Recalled by...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS System (HCP) The CoaguChek XS System is intended Recalled by...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.