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. 2,536 recalls have been distributed to New Hampshire in the last 12 months.
Showing 8301–8320 of 49,311 recalls
Recalled Item: Digisonics OBView Versions 4.8.2 SP6 - 4.8.3 Recalled by Digisonics, Inc Due...
The Issue: Software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tydemy (drospirenone Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Stability Specification and Failed Impurities/Degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough...
The Issue: CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe Tussin PM Night Time Cough Relief (Cough Suppressant/Antihistamine)...
The Issue: CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PANCREAZE (pancrelipase) Delayed-Release Capsules Recalled by Vivus, Inc....
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tizanidine Tablets Recalled by Amerisource Health Services LLC Due to Failed...
The Issue: Failed Dissolution Specifications: this repackaged product was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1/2 gallon CN Smith brand Apple Cider Recalled by Bevovations, LLC Due to...
The Issue: Product contains high levels of patulin (above 50ppb).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: UroLift Visual Obturator Recalled by Scholly Fiberoptic Gmbh Due to There is...
The Issue: There is an improperly performed weld between the cone of the sheath lock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellacor System with Micro-Coring Technology-Indicated for use by medical...
The Issue: Potential failure of a bearing adhesive joint that can occur due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes and Surgical Room Turnover (SRT) Kits: Recalled...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINEAR 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION 7 Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YAMATO PLUS IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 7.5Fr IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANS-RAY IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REINFORCED INTRODUCER SET Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 8Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 8Fr. IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.