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 18441–18460 of 27,899 recalls
Recalled Item: GrebSet Micro-Introducer Kit Recalled by Vascular Solutions, Inc. Due to...
The Issue: Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor Recalled by Physio-Control, Inc. Due to The firm has...
The Issue: The firm has become aware of a potential device issue where the LIFEPAK 15...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Latex HCY REAGENT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: The firm confirmed a reduced once-opened and on-board stability for N Latex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...
The Issue: Firm received a complaint of the tip holder breaking during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular catheter introduction kit The PICC is indicated for short Recalled...
The Issue: There have been complaints for peel away sheaths flaring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration full Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Software error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...
The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...
The Issue: Incorrect dose after editing beam number an wedge angle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee Tibial Insert Recalled by Encore Medical, Lp Due to The...
The Issue: The Empowr PS Insert was reported as missing the impaction slot feature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The...
The Issue: Lima Proximal Bodies were inadvertently re-sterilized. The safety screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GN200 Caiman HF generators Recalled by Aesculap Implant Systems LLC Due to...
The Issue: Generators may have a faulty component which could impact the proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) has identified that in a rare sequence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...
The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) VANTA¿ XRF...
The Issue: It was discovered under rare circumstances the LED warning light circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...
The Issue: Products were made outside of Quality System Regulation, and potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System - C-Spine Coil Recalled by Hitachi Medical Systems...
The Issue: The customer indicated that the coil balun was hot to the touch when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color contact lenses labeled under the following brands: Diamond Recalled by...
The Issue: Sterility and Misbranding: Lenses may not be sterile and may be labeled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.