Home / Recalls / Synergetics Inc / Z-2254-2024

Z-2254-2024 Class I Ongoing

Recalled by Synergetics Inc — O Fallon, MO

Recall Details

Product Type
Devices
Report Date
July 17, 2024
Initiation Date
June 12, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
35 units

Product Description

BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)

Reason for Recall

Sterilization certificates could not be validated by the supplier

Distribution Pattern

US Nationwide

Code Information

UDI/DI 20841305107612, Lot Number P62764970R

Other recalls by Synergetics Inc

  • Z-2251-2024 Class I — BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravit (June 12, 2024)
  • Z-2252-2024 Class I — BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration (June 12, 2024)
  • Z-2253-2024 Class I — BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of (June 12, 2024)
  • Z-0119-2017 Class II — 25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E (August 11, 2016)
  • Z-0120-2017 Class II — 25 gauge VersaVit 2.0 Procedure Pack with Mid-Field Illuminator, Product/Part Nu (August 11, 2016)
  • Z-0122-2017 Class II — 25 gauge VersaVit 2.0 Vitrectomy Cutter, Product/Part Number 70935, packaged in (August 11, 2016)
  • Z-0121-2017 Class II — 25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator, Product (August 11, 2016)
  • Z-0897-2014 Class II — 25ga Mid-Field Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.22 (December 9, 2013)
  • Z-0898-2014 Class II — 23ga Aspirating Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.2 (December 9, 2013)
  • Z-0899-2014 Class II — 25ga Aspirating Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.2 (December 9, 2013)