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. 2,558 recalls have been distributed to New Hampshire in the last 12 months.
Showing 4941–4960 of 49,311 recalls
Recalled Item: Disposable 5 Lead Cable and Lead Wire System Recalled by Stryker...
The Issue: Disposable 5 lead cable and lead wire system package that should contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max- Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multitom Rax -Intended to visualize anatomical structures by converting an...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis Recalled by...
The Issue: Affected product has an increased risk of postoperative perisprosthetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling
The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fludrocortisone Acetate Tablets Recalled by Teva Pharmaceuticals USA, Inc...
The Issue: Failed Impurities/Degradation Specifications: Product is being recalled due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Failed Dissolution Specifications: results below specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PST 500 U Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX450 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX550 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamond Shruumz Chocolate Bars Dark Chocolate Recalled by Prophet Premium...
The Issue: Toxic levels of muscimol
Recommended Action: Do not consume. Return to store for a refund or discard.