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 25601–25620 of 27,899 recalls
Recalled Item: Medtronic SynchroMed EL Programmable pumps Recalled by Medtronic...
The Issue: Medtronic is providing Healthcare Professionals with important safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Sutureless Pump Connector Revision Kit Recalled by Medtronic...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intrathecal Catheter Pump Segment Revision Kit Recalled by...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Vector Distractor Pin Holding Clamp Recalled by Synthes USA HQ, Inc....
The Issue: Synthes is initiating a voluntary Medical Device removal for specified part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX Instrument Recalled by Becton Dickinson & Co. Due to Electrical power...
The Issue: Electrical power module installed on some in vitro diagnostic instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Recalled by...
The Issue: The firm is initiating a Field Safety Correction for the labeling of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...
The Issue: When the bed is put into the chair egress position, the magnets on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO-MED ORTHO TOTAL JOINT TRACECART(R) Recalled by DeRoyal Industries Inc...
The Issue: DeRoyal recalled kits that contained Stryker togas which were recalled for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******QTY 1***APEX Arthroscopy Tubing Set. Intended for use for Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Glidesheath (tm) Recalled by Terumo Medical Corporation Due to...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large Recalled by...
The Issue: Stryker has received reports from customers indicating post-operative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The information regarding the FILM Mode calibration may have been considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...
The Issue: Product labeled with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.