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. 2,409 recalls have been distributed to New Hampshire in the last 12 months.
Showing 18301–18320 of 49,311 recalls
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Product...
The Issue: Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oscar 2 Recalled by Suntech Medical, Inc. Due to The device display, when...
The Issue: The device display, when activated, can show an incorrect decimal point when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....
The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: Recalled...
The Issue: One (1) TRUE METRIX AIR blood glucose meter distributed in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are...
The Issue: Internal Paddles may wear over time and may not be safe or ready for use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B Recalled by...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Urine Drug Control Recalled by Cardinal Health Inc. Due to...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-Hydroxybutyrate LiquiColor Recalled by Cardinal Health Inc. Due to Three...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strep B Carrot Broth One-Step Recalled by Cardinal Health Inc. Due to Three...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha VA30-mobile X-Ray system Recalled by Siemens Medical...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha VA20-mobile X-Ray system Material # 10308191 The Recalled...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Spin VA30-mobile X-Ray system Recalled by Siemens Medical...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftazidime for Injection USP and Dextrose for Injection USP Recalled by B....
The Issue: Failed Stability Specifications: Out-of-Specification (OOS) results for High...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acrysof Recalled by Alcon Research LLC Due to Incorrect IOL diopter
The Issue: Incorrect IOL diopter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Low Weight-Low Volume Blood Transport System for...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.