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. 1,670 recalls have been distributed to New Hampshire in the last 12 months.
Showing 43241–43260 of 49,311 recalls
Recalled Item: Stryker brand COMPLIANT 4MM X 20MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 30MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 4MM X 10MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand GDC-10 ULTRA SOFT 2MM X 3CM Recalled by Stryker Neurovascular...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED 45 150CM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 15MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand GDC VORTX 2MM X 3MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED S 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand SUPER COMPLIANT 4MM X 7MM Recalled by Stryker Neurovascular...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 4MM X 15MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR 1018 PRE-SHAPED 45 150CM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED C 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split...
The Issue: Lanx, Inc. is recalling various lots of Timberline MPF Straight Split Tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dekompressor Percutaneous Discectomy Probe. The Dekompressor is a single use...
The Issue: Stryker has identified a potential for the auger and/or cannula to fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glucotrol XL (glipizide) extended release tablets Recalled by Pfizer Inc....
The Issue: Failed Dissolution Specification; 8 hr stability timepoint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydravax High Potency Diuretic Weight Loss Solution Recalled by IQ...
The Issue: Marketed Without an Approved NDA/ANDA; this product is being recalled for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Soliris (eculizumab) Concentrated Solution for Intravenous Infusion Only...
The Issue: Presence of Particulate Matter: Failed the appearance test for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide XL (glipizide) extended release tablets Recalled by Greenstone Llc...
The Issue: Failed Dissolution Specification; the bulk lot yielded an out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.