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. 2,534 recalls have been distributed to New Hampshire in the last 12 months.
Showing 10401–10420 of 27,899 recalls
Recalled Item: BD Phoenix PMIC/ID-105: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas pro integrated solutions (cobas pro ISE Recalled by Roche...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-110: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas 8000 modular analyzer series (i.e. Recalled by Roche Diagnostics...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** COX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due to...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** spineX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** SHEEHY BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOLMaster 700 Recalled by Carl Zeiss Meditec AG Due to When using software...
The Issue: When using software 1.90.2.09 or 1.90.8.06 and using modality worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: visby medical COVID-19 Test kit *** An in vitro diagnostic Recalled by VISBY...
The Issue: Two issues: 1) 5 Lots were found to have incorrect labeling on the outer box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Medela .0193 AXS Universal Aspiration Tubing (01)07612367053921 -...
The Issue: Incorrect expiration date of "2023-07-24" on label of sterile tubing....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60" (152 cm) Appx 1.9 ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 154 cm (61 IN) APPX 1.5ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7 IN (18cm) APPX 0.43ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60 IN (152cm) APPX 1.5 ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.