Lacrimedics Inc: Medical Device Recall in 2022 - (Recall #: Z-0709-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Collagen Plugs, CP3, 0.3mm, CP4, 0.4mm, CP5, 0.5 mm, Sterile, EO, Rx Only, CE Dry eye treatment

Product Classification:

Class II

Date Initiated: January 17, 2022

Date Posted: March 9, 2022

Recall Number: Z-0709-2022

Event ID: 89463

Reason for Recall:

The sterile pouch seal may contain channels that could affect the seal integrity and potentially compromise sterility.

Status: Ongoing

Product Quantity: 4780 units

Code Information:

CP3 010421-3358 CP3 031419-3125 CP3 032921-3429 CP3 042020-3284 CP3 052219-3149 CP3 061521-3482 CP3 071720-3322 CP3 080218-3045 CP3 091218-3057 CP3 122118-3093 CP4 010621-3377 CP4 022619-3094 CP4 041620-3285 CP4 041719-3126 CP4 072020-3323 CP4 092518-3058 CP5 011221-3359 CP5 033121-3430 CP5 042219-3127 CP5 042220-3286 CP5 072320-3324 CP5 082318-3010 CP5 111418-3059 HP7 103018-3062

Distribution Pattern:

Nationwide and Worldwide Distribution to following countries - AR. BE, BO, BR, CH, CN, CO, CZ, DE, EC, ES, FI, GE, IN, IL, MY, MX, NZ, PE, RO, SG, SA, TR, TW, TZ, UK

Voluntary or Mandated:

Voluntary: Firm initiated