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. 952 recalls have been distributed to New Hampshire in the last 12 months.
Showing 37961–37980 of 49,311 recalls
Recalled Item: 113" (287cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipo Pack Recalled by Stradis Healthcare, LLC. Due to Convenience kits being...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Systems LOCI Thyroid Stimulating Hormone Recalled by Siemens...
The Issue: Dimension Vista LOCI Thyroid Stimulating Hormone (TSH) Lot 14237AA may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaginal Rejuvenation Pack - contains Devon Light Glove Used during surgery...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Arthro Pack and Knee Arthro Pack II - contains Recalled by Stradis...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 127" (323cm) Transfer Set w/Check Valve Recalled by ICU Medical, Inc. Due to...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suction Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IC-GREEN (indocyanine green for injection Recalled by Akorn, Inc. Due to...
The Issue: Subpotent Drug: Low out-of-specification potency result of the drug product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...
The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Librax (5 mg chlordiazepoxide HCl and 2.5 mg clidinium bromide) capsules...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlordiazepoxide HCl/Clidinium Bromide capsules Recalled by Valeant...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: High out of specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...
The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...
The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MCK Maximum Congruent Knee System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Basin Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.