New Hampshire recalls
3270 federal recalls on file affecting New Hampshire - 195 New Hampshire-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-25FDA-DeviceMedlineClass IINationwideStop using Medline Lithotomy Pack kits
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical kits for sterilization defects
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline endoscopy kits for sterilization defect
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideMedline Convenience Kits: 1) MAJOR LAPAROTOMY CDS, Model Number: CDS860015U; 2) MAJOR LAPAROTOMY CDS, Model Number: CDS860015V; 3) MAJOR LAPAROTOMY CDS, Model Number: CDS860015W; 4) MAJOR LAPAROTOMY CDS, Model Number: CDS860015X; 5) MINOR LAPAROTOMY CDS, Model Number: CDS860016P; 6) MINOR LAPAROTOMY CDS, Model Number: CDS860016Q; 7) MINOR LAPAROTOMY CDS, Model Number: CDS860016R; 8) MINOR LAPAROTOMY CDS, Model Number: CDS860016S; 9) LAP GASTRIC BYPASS CDS, Model Number: CDS86014
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical kits for sterilization issues
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck your Medline Dental Pack lot number
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical and biopsy kits for lot numbers
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical kits for sterilization concerns
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical kits for sterilization concerns
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical kits for sterilization problems
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical kits for lot numbers
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideStop using Medline nerve block trays
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideReturn Medline Convenience Kits to your supplier
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline tracheostomy kits for recall
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedlineClass IINationwideCheck Medline surgical kits for proper sterilization
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceAuris HealthClass IINationwideStop using affected Auris Health MONARCH devices
Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading, application will re-initialize to patient-left position; and if right position was previously selected, this may lead to unanticipated robotic arm positioning toward patient-left, may result in contact with patient/endotracheal tube.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical devices
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat 5mm instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat devices
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceMedicaClass IINationwideStop using Medica capillary tubes
A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes.
- 2026-02-25FDA-DeviceImmunotechClass IINationwideStop using Immunotech Estrone RIA kits
The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.
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