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. 2,278 recalls have been distributed to New Hampshire in the last 12 months.
Showing 47441–47460 of 49,311 recalls
Recalled Item: Daily Balance Vanilla Dietary Supplement Packaged under the labels Stronger...
The Issue: Protein supplement fails to declare allergen milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Endurance Pre Race Pina Colada Recalled by Maine Natural Health, Inc. Due to...
The Issue: Protein supplement fails to declare allergens: milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Endurance Daily Chocolate Dietary Supplement Packaged under the label:...
The Issue: Protein supplement fails to declare allergens milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Recovery Vanilla (also labeled Post Workout) Recalled by Maine Natural...
The Issue: Protein supplement fails to declare allergens: milk, shellfish
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SLIM XTREME Herbal Slimming Capsule Recalled by Globe All Wellness, LLC Due...
The Issue: Marketed Without an Approved NDA/ANDA: Product tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL...
The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL...
The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Cetirizine HCl Chewable Tablets 5 mg Recalled by Sandoz...
The Issue: Impurity/Degradation; exceeded impurity specification at the 8 and 15 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alden's Cookies and Cream is an ice cream product. It Recalled by Oregon Ice...
The Issue: Alden's Cookies and Cream was packaged in the wrong cup and a correct lid...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware that patient mismatch without a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TM Ardis Interbody System Inserter Stainless Steel Recalled by Zimmer,...
The Issue: Zimmer Spine is has received complaints of difficulty in turning the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA ML Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX PENTRA ML because they have confirmed an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...
The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...
The Issue: The Back Table Cover component in the custom pack was placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CapLOX II Final Torque Driver Recalled by Captiva Spine, Inc Due to Captiva...
The Issue: Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...
The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 200amx with digital upgrade Mobile general Recalled...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima 200amx Mobile general purpose radiographic imaging of...
The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.