Alabama recalls
4377 federal recalls on file affecting Alabama - 369 Alabama-specific plus 4008 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed Carestation recalled for fastener hazard
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
- 2026-06-24FDA-DeviceGEClass IINationwideGE Giraffe OmniBed recalled for loose fastener risk
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert issue
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal surgical trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal access port recalled for overpressure alerts
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceConMedClass IINationwideConMed AirSeal trocar recalled for overpressure alert risk
Potential for overpressure alerts.
- 2026-06-24FDA-DeviceHowmedica OsteonicsClass IINationwideHowmedica Triathlon Baseplate Size 3 recalled for mislabeling
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).
- 2026-06-24FDA-DeviceAccriva DiagnosticsClass IINationwideAccriva directCHECK quality control recalled for incorrect labeling
Assayed Whole blood control contains labeling with incorrect performance range.
- 2026-06-24FDA-DeviceMedtronicClass IINationwideMedtronic O-arm O2 recalled for image artifact risk
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.
- 2026-06-24FDA-DeviceSterisClass IINationwideSteris ALYON surgical lights recalled for detachable buttons
The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
- 2026-06-24FDA-DeviceSterisClass IINationwideSteris HarmonyAIR surgical lights recalled for detachable buttons
The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
- 2026-06-24FDA-DeviceSterisClass IINationwideSteris HarmonyAIR surgical lights recalled for paint chipping
There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline hysterectomy kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline C-section kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline arterial insertion and PICC dressing kits recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for defective adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline port-a-cath kits recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline femoral block tray kits recalled for tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline medical kits recalled for cracked adhesive tubing
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline CVC insertion kits recalled for tubing failure
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline dressing change kits recalled for adhesive tubing defect
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- 2026-06-24FDA-DeviceMedlineClass IINationwideMedline Centurion kits recalled for tubing crack risk
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
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