Home / Recalls / Delta Med SpA / Z-2295-2021

Z-2295-2021 Class II Ongoing

Recalled by Delta Med SpA — Viadana, N/A

Recall Details

Product Type
Devices
Report Date
August 25, 2021
Initiation Date
June 21, 2021
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
30,900 units

Product Description

DELTAVEN Safety I.V. Catheter in Pur with closed system: a) REF 3836272 b) REF 3814272 c) REF 3845272 d) REF 3856272

Reason for Recall

Problems related to the sterilization of the medical devices; possible missing sterility of the medical device

Distribution Pattern

US Nationwide distribution in the states of FL and MN.

Code Information

a) REF 3836272, Lot 11T80188 b) REF 3814272, Lot 11T80272 c) REF 3845272, Lot 12T80147 d) REF 3856272, Lot 12T80347

Other recalls by Delta Med SpA

  • Z-2299-2021 Class II — NEO DELTA Self Safe, I.V. Catheter REF 3738222 (June 21, 2021)
  • Z-2303-2021 Class II — NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822 (June 21, 2021)
  • Z-2297-2021 Class II — DELTAVEN FASTFLASH, Safety I.V. Catheter in Pur with closed system: a) REF 3814 (June 21, 2021)
  • Z-2296-2021 Class II — DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 (June 21, 2021)
  • Z-2304-2021 Class II — NEO DELTA SELFSAFE PUR T, I.V. Catheter: (June 21, 2021)
  • Z-2298-2021 Class II — DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) R (June 21, 2021)
  • Z-2305-2021 Class II — WOLF-PAK Self Safe Safety IV Catheter: a) REF PIVD2010W b) REF PIV2210W c) RE (June 21, 2021)
  • Z-2300-2021 Class II — NEO DELTA Self Safe 1, I.V. Catheter with PUR REF 3708122, Lot 00A1160627 5000 (June 21, 2021)
  • Z-2301-2021 Class II — NEO DELTA Self Safe T, I.V. catheter of PUR a) REF 3779422 b) REF 3769522 c) (June 21, 2021)
  • Z-2302-2021 Class II — NEO DELTA SELFSAFE PUR 1, I.V. Catheter, REF 3718122 (June 21, 2021)