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# Bausch+Lomb Recalls I-Pack Injection Kit
- URL: https://www.fdaweb.com/bausch-lomb-recalls-i-pack-injection-kit/
- Published: 2024-07-12T12:00:00.000Z
- Updated: 2026-09-14T14:35:20.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157344

Bausch+Lomb’s Synergetics unit is recalling (Class 1) its I-PACK Injection Kit with Drape, which is used for the administration of an intravitreal (back of the eye) injection, because sterilization certificates could not be validated by the supplier. The company sent an “Urgent Medical Device Voluntary Recall” notice to its consignees on 5/12, which explained the issue, potential hazard, and requested that affected inventory be isolated to prevent unintended use, according to a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=208338&ref=fdaweb.com).