Lacrimedics Inc: Medical Device Recall in 2022 - (Recall #: Z-0708-2022)

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:

OPAQUE Herrick Lacrimal Plugs, HP3, 0.3 mm, HP5, 0.5mm, HP7, 0.7.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-0708-2022

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: 5767 units

Code Information:

HP3 010819-3104 HP3 011321-3373 HP3 031519-3128 HP3 032521-3426 HP3 051419-3157 HP3 073118-3044 HP3 090921-3516 HP3 102618-3060 HP5 011221-3374 HP5 012519-3088 HP5 032019-3123 HP5 032621-3425 HP5 051519-3158 HP5 062521-3489 HP5 070819-3186 HP5 072221-3501 HP5 083018-3036 HP5 102918-3061 HP5 122120-3368 HP7 030821-3404 HP7 032119-3124 HP7 092019-3135 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