FDAFDA · Alimentos y medicamentos·N.º oficial Z-1113-2024
Medline Kits, trays, and packs labeled as follows: a) PORT ACCESS TRAY, REF DYNDA2863; b) PORT ACCESS TRAY, REF DYNDA2863H; c) ULTRASOUND GUIDED IV START KIT, REF DYNDV2518; d) ULTRASOUND GUIDED IV START KIT, REF DYNDV2518H; e) KIT ULTRASOUND PIV START, REF DYNDV2445; f) NICU INSERTION & DRSG CHG TRAY, REF EBSI1306A; g) PIV BSI KIT, REF BSIPIV1010; h) ULTRASOUND GUIDED IV START KIT, REF DYNDV2465
Publicado el 6 de marzo de 2024 · Inicio del retiro: 15 de noviembre de 2023
Estado reportado al momento de publicación: Ongoing — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.
Qué peligro representa
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Qué hacer
Voluntary: Firm initiated · Letter
Detalles del retiro
- Fabricante
- MEDLINE INDUSTRIES, LP - Northfield
- Distribuidor
- Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama
- Lote
- a) REF DYNDA2863, UDI/DI 40195327008025 (case), 10195327008024 (unit), Lot Numbers: 22ABQ171, 22ABT619, 22IBG373; b) REF DYNDA2863H, UDI/DI 40195327008025 (case), 10195327008024 (unit), Lot Numbers: 22ABQ171, 22ABT619, 22IBG373; c) REF DYNDV2518, UDI/DI 40195327089079 (case), 10195327089078 (unit), Lot Numbers: 22GBA169, 22HBU208; d) REF DYNDV2518H, UDI/DI 40195327089079 (case), 10195327089078 (unit), Lot Numbers: 22GBA169, 22HBU208; e) REF DYNDV2445, UDI/DI 20193489110576 (case), 10193489110579 (unit), Lot Numbers: 2022012480; f) REF EBSI1306A, UDI/DI 00653160352122 (case), 10653160352129 (unit), Lot Numbers: 2022042850; g) REF BSIPIV1010, UDI/DI 00653160349153 (case), 10653160349150 (unit), Lot Numbers: 2022020750, 2022040480, 2022082980; h) REF DYNDV2465, UDI/DI 20193489110163 (case), 10193489110166 (unit), Lot Numbers: 2022031480, 2022041880
- Clasificación de riesgo
- Class I
- Área (FDA)
- device
- País
- United States
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