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. 2,367 recalls have been distributed to New Hampshire in the last 12 months.
Showing 28161–28180 of 49,311 recalls
Recalled Item: Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879 Recalled by...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw Driver. Part of MAXIMIS Pedicle Screw Recalled...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 5.5 x 55mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 40mm Straight Rod. Part of MAXIMIS Pedicle Screw Recalled...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 5.5 x 45mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Extension Sleeve. Part of MAXIMIS Pedicle Screw Spinal...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Persuader. Part of MAXIMIS Pedicle Screw Spinal Fixation...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Extension Driver. Part of MAXIMIS Pedicle Screw Spinal...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Unit Abutment Angled Recalled by Keystone Dental Inc Due to Abutments...
The Issue: Abutments are unable to accept the final abutment screw
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...
The Issue: The firm has identified that a fitting in some Slidemaker Stainer units may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary Recalled by ConMed...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Recalled by...
The Issue: Software- scheduled A-QC analysis could initiate prior to a patient result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Succinylcholine Chloride Recalled by Fagron Compounding Services LLC dba...
The Issue: Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ibuprofen Tablets Recalled by Time-Cap Laboratories, Inc. Due to Presence of...
The Issue: Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.