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. 2,292 recalls have been distributed to New Hampshire in the last 12 months.
Showing 40741–40760 of 49,311 recalls
Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...
The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas IT 1000 Product Usage: Intended Use: An electronic Recalled by...
The Issue: Potential that test results would be assigned to the wrong Patient ID if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility; complaints of mold in the overpouch
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Depo-Medrol (methylprednisolone acetate injectable suspension USP) Recalled...
The Issue: Failed pH Specification: A pH result of 2.9 was obtained at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cataflam (diclofenac potassium) tablets Recalled by Novartis Pharmaceuticals...
The Issue: Failed Tablet/Capsule Specifications: Ink identification had rubbed off...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...
The Issue: Internal review found that five (5) PFJ implant forgings were identified as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: The product was discolored and contained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sunburst SUPERFOODS ORGANIC RAW CAROB POWDER in ONE POUND and Recalled by...
The Issue: The repacked product has the potential to be contaminated with Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OXYCODONE HYDROCHLORIDE C II Oral Solution USP Recalled by Boehringer...
The Issue: Failed Stability Specifications: Out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Symbia T Series consists of the T16 Recalled by Siemens Medical...
The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbia Intevo series consists of the Intevo 16 Recalled by Siemens...
The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.