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. 1,102 recalls have been distributed to New Hampshire in the last 12 months.
Showing 2121–2140 of 49,311 recalls
Recalled Item: VITROS Chemistry Products CHE Slides Recalled by Ortho-Clinical Diagnostics,...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Plains Bentonite + Herbal Detox Capsules 60 capsules Recalled by Yerba...
The Issue: Potential contamination with Pseudomonas aeruginosa.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIMMTRAK (tebentafusp-tebn) Injection Recalled by IMMUNOCORE, LLC Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...
The Issue: As a result of a comprehensive product performance review it was determine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZICAM NASAL ALLCLEAR Recalled by Church & Dwight Inc Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZICAM COLD REMEDY MEDICATED NASAL SWABS Recalled by Church & Dwight Inc Due...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orajel Baby Recalled by Church & Dwight Inc Due to Microbial Contamination...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Custom Tubing Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Pressure Tubing: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Manifold Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Waste Management Kit: Recalled by Merit Medical Systems, Inc. Due to...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Recalled by DRG...
The Issue: An incoming complaint reported that the expiration date on the kit box label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zvu Anorectal Manometry Procedure Kit Recalled by Diversatek Healthcare Due...
The Issue: Anorectal manometry procedure kit outer kit label is mislabeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.