Every recall we track for Synergetics Inc — 4 in all — plus the complaints and injury reports the public filed about them.
BAUSCH+LOMB I-PACK Injection Kit Custom REF 18069 recalled due to unverified sterilization certificates. Affected units may pose infection risks during eye injections.
BAUSCH+LOMB I-PACK Injection Kit with Wire Speculum (REF 18069W) recalled due to unverified sterilization certificates. This device is used for eye injections and may pose risks if not properly sterilized.
Synergetics Inc recalls BAUSCH+LOMB I-PACK Injection Kit with Drape REF 18061 due to unvalidated sterilization certificates. This affects intravitreal injection kits sold with UDI/DI 20841305107551 and Lot P63044983R.
Synergetics Inc recalls BAUSCH+LOMB I-PACK Injection Kit REF 18060 due to unverified sterilization certificates. This affects intravitreal eye injections. Contact for details.
