Data Foundry

Medical device recalls 2017

PGCL [poly — Class II medical device recall Z-1872-2017

Ongoing recall by CP Medical Inc, reported 2017-04-26, distributed in AL, AR, AZ, CA, CO, CT, FL, ID…. The tensile strength minimum as directed by USP <881> was not met over the length of the product's shelf life.

Recall numberZ-1872-2017
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCP Medical Inc, Norcross, GA, United States
Recall initiated2017-02-02
Classified2017-04-20
Reported by FDA2017-04-26
DistributedAL, AR, AZ, CA, CO, CT, FL, ID, IL, IN, KY, LA, MT, NE, NJ, NM, NY, OK, OR, SC, TX, WA
Countries outside the USZA
Reason classespotency
Lot numbers150323-04, 150324-04, 150520-10, 150615-01, 150616-08, 150709-01, 151229-64, 160414-69, 160510-59, 160617-52, 160824-50

Product

PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes L923, L459, L493, L762, L463, L922, L495, L463, L497, L494, L493

Reason for recall

The tensile strength minimum as directed by USP <881> was not met over the length of the product's shelf life.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1872-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.