New York recalls
5074 federal recalls on file affecting New York - 1064 New York-specific plus 4010 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 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.
- 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 convenience 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 convenience kits recalled for cracked 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 LAVH 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 C-section 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 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 pelviscopy kit 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 delivery kit 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 neuro kits recalled for defective adhesive
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 hernia repair tote 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 dressing change kit recalled for defective 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 IV Start Kit 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
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 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 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 convenience 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.
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