Every recall we track for Mani, Inc. - Kiyohara Facility — 3 in all — plus the complaints and injury reports the public filed about them.
Mani recalls two trocar kit models (MTK23S and MTK25S) due to potential packaging defects that could compromise sterile barriers. Affected kits were sold with specific lot numbers and expiration dates.
Mani recalls TROCAR KIT 23G S used in eye surgery due to Luer connector dimensions causing fluid leakage and unintended disconnection during ophthalmic procedures.
Mani recalls 23G S infusion cannulas for eye surgery due to potential fluid leakage and disconnection risks. Affected units have specific lot codes and expiration dates.
