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. 2,364 recalls have been distributed to New Hampshire in the last 12 months.
Showing 29381–29400 of 49,311 recalls
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...
The Issue: PEG kits have the potential for one of the following defects: missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...
The Issue: PEG kits have the potential for one of the following defects: missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Stealth Chamber Recalled by Iba Dosimetry Due to When the Stealth...
The Issue: When the Stealth Chamber is used as a detector in relative dosimetry,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffmann LRF Safety Clip (Bone Transport Strut) Recalled by Stryker...
The Issue: Stryker is recalling Hoffmann LRF (Limb Reconstruction Frame) System Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venture RX Catheter Recalled by Vascular Solutions, Inc. Due to Vascular...
The Issue: Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarke-Reich Laparoscopic Knot Pusher Recalled by Cook Inc. Due to...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Introducer/Extractor Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra-Raz Ligature Carrier Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra Ligature Carrier 75 Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ IV Premium Catheter Stabilization Device Recalled by Bard Access...
The Issue: StatLockTM IV Premium Catheter Stabilization Device may contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST ETP32 (Ertapenem) Ref. 531640 Recalled by BioMerieux SA Due to False...
The Issue: False susceptible results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Microalbumin Reagent Recalled by Beckman Coulter Inc. Due to Beckman Coulter...
The Issue: Beckman Coulter has confirmed that MA Reagent Lot M609458 may recover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brennen Skin Graft Mesher. Surgical instrument designed to expand skin...
The Issue: Sterilization validation failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.