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. 2,330 recalls have been distributed to New Hampshire in the last 12 months.
Showing 36401–36420 of 49,311 recalls
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code...
The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for z-statistic related to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doubletree Cookie Dough Recalled by Christie Cookie Co Inc Due to Reports of...
The Issue: Reports of clear and green plastic pieces in cookies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due...
The Issue: EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TESTOSTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROGESTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METHIONINE/CHOLINE/INOSITOL Recalled by JD & SN Inc., dba Moses Lake...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPAVERINE/PHENTOLAMINE Recalled by JD & SN Inc., dba Moses Lake...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROXYPROGESTERONE CAPROATE OIL Recalled by JD & SN Inc., dba Moses Lake...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.