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. 2,476 recalls have been distributed to New Hampshire in the last 12 months.
Showing 14541–14560 of 27,899 recalls
Recalled Item: Maximum Variable Pitch Compression Tray Base Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for silicone shedding during cleaning and sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant....
The Issue: The surgical technique is being updated to caution against misuse due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESERVOIR "Y" ADAPTER Recalled by Medtronic Perfusion Systems Due to...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Recalled...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 4x5 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Recalled by Philips North America LLC Due to Affected...
The Issue: Affected lithium-ion batteries may contain a defective component (Thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...
The Issue: The device is unable to pair with the mobile app due to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to...
The Issue: Potentially lead to anchor breakage during insertion,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model...
The Issue: HVAD Battery Charger units manufactured with wrong inductors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireSR Recalled by LivaNova USA Inc Due to This...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireHC Model 105 Generator Recalled by LivaNova USA...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LivaNova VNS Therapy System Recalled by LivaNova USA Inc Due to Lead...
The Issue: Lead impedance values reported by the affected VNS generator will be higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare 9805 and 9805P Hydraulic Patient Lifts Recalled by Invacare...
The Issue: Invacare has identified via customer complaints, the potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...
The Issue: Labeling error. The product is labeled with an 18 month expiration date,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various GE Magnetic Resonance System on-site software version Product Usage:...
The Issue: Possible incorrect software version loaded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....
The Issue: Incorrect expiry date of 17-Dec-19 Correct expiry date is 11-Aug-19
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....
The Issue: Incorrect expiry date of 9-Feb-20 Correct expiry date is 30-Aug-19
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.