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. 2,508 recalls have been distributed to New Hampshire in the last 12 months.
Showing 11961–11980 of 27,899 recalls
Recalled Item: Jamshidi Bone Marrow Biopsy/Aspiration Needle Recalled by Bard Peripheral...
The Issue: Sterility compromised due to packaging pouches that may not be sealed properly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter 6F Model 5540. For delivery of Recalled by...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit Recalled by Avanos...
The Issue: The CORFLO PEG tube may become blocked at the center of the adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncomine Dx Target Test DNA Control-IVD for detection of DNA Recalled by...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of Recalled by Life...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ion Torrent Dx No Template Control Kit- IVD for detection Recalled by Life...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncomine Dx Target Test RNA Control- IVD for detection of Recalled by Life...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Recalled by...
The Issue: A high frequency output (2 MHz) has not been cleared for distribution in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips...
The Issue: There were unknown bioburden levels prior to sterilization, which may affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description:...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. Recalled by...
The Issue: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreludeSYNC DISTAL Radial Compression Devices Recalled by Merit Medical...
The Issue: During the sterilization of radial compression devices, some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...
The Issue: Updated Instructions For Use- to contraindications and potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...
The Issue: Intermittent failure of a signal being sent to a monitor from the touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...
The Issue: As part of an investigation into a biocompatibility test discrepancy where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOLITH URO-TCH 9FR PROBE 54CM Recalled by Northgate Technologies, Inc. Due...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products TT4 Reagent Pack Recalled by Ortho Clinical...
The Issue: The specified reagent packs exhibit an increase in the frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 FLEX Recalled by Radiometer Medical ApS Due to Analyzer's barcode...
The Issue: Analyzer's barcode reader misinterprets the contents of barcode label used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.