Synergetics Inc: Medical Device Recall in 2024 - (Recall #: Z-2252-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)

Product Classification:

Class I

Date Initiated: June 12, 2024

Date Posted: July 17, 2024

Recall Number: Z-2252-2024

Event ID: 94793

Reason for Recall:

Sterilization certificates could not be validated by the supplier

Status: Ongoing

Product Quantity: 2 units

Code Information:

UDI/DI 20841305107551, Lot Number P63044983R

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated