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. 2,552 recalls have been distributed to New Hampshire in the last 12 months.
Showing 5941–5960 of 49,311 recalls
Recalled Item: Brand Name: Dako CoverStainer Recalled by Agilent Technologies Due to There...
The Issue: There is the potential for the front plexiglass door of the automated slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage Recalled by Andover...
The Issue: A packaging seal gap could impact the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Humidifier Recalled by Fisher & Paykel Healthcare, Ltd. Due to...
The Issue: Humidifier devices, used to deliver high flow respiratory therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124...
The Issue: Device may experience an interruption or loss of therapy in case of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER Application Instrument Recalled by Karl Storz Endoscopy Due to Laser...
The Issue: Laser surgical instruments have no specific evidence of a validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eyesaline Recalled by HONEYWELL INC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version:...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oncology Essentials Package of the Spectral CT imaging system. Recalled...
The Issue: Potential for third party oncology marking laser to be off the gantry cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1 Recalled by Stryker Leibinger GmbH & Co. KG Due to Mislabeling
The Issue: Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atovaquone Oral Suspension USP Recalled by AvKARE Due to Microbial...
The Issue: Microbial contamination of a non-sterile product: potential Bacillus cereus...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isotretinoin Capsules Recalled by Teva Pharmaceuticals USA, Inc Due to...
The Issue: Superpotent Drug: The 3-month stability result for assay was found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HORIBA custom configured fluorescence instrument Recalled by Horiba...
The Issue: HORIBA custom configured fluorescence instrument has a laser safety defect....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 13.0.0.1547 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 8.1.0.47 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9.0.0.113 and 9.0.1.142. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 11.0.0.951 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 8.0.0.61 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 15.0.0.430. Radiation Therapy Treatment Planning System. Recalled...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 7.0.0.19. Radiation Therapy Treatment Planning System. Recalled...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.