Data Foundry

Medical device recalls 2014

Surgical packs — Class I medical device recall Z-0237-2015

Terminated recall by Customed, Inc, reported 2014-12-10, distributed in FL, NY, PR. Customed products are being recalled because of compromised sterility, not limited to potentially damaged pack

Recall numberZ-0237-2015
Product typeMedical device
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCustomed, Inc, Fajardo, PR, United States
Recall initiated2014-10-08
Classified2014-11-28
Reported by FDA2014-12-10
Terminated2017-08-14
DistributedFL, NY, PR
Quantity185,000
Reason classessterility
Lot numbers111102811, 111112953, 111112969, 111123257, 111123438, 112010003, 112020291, 112030762, 112041051, 112041384, 112051641, 112051718, 112062298, 112072758, 112083040, 112104122, 112104289, 112114540, 112124364, 112124885, 113025838, 113026102, 113026206, 113057390, 113057682, 113099556, 131010023, 131210663, 140111103, 140412874, 140513047, 140513388, 140613946, 140714499, 140815022

Product

Surgical packs (includes trays, bags and kits) Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

Reason for recall

Customed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes (QSR) and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.

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-0237-2015. 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.