FDA Medical Device Recalls (openFDA)
Customed, Inc: CESAREAN PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
- Recall number
- Z-2672-2015
- Recalling firm
- Customed, Inc
- Product
- CESAREAN PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
- Status
- Terminated
- Initiated
- 2015-07-10
- Posted
- 2015-09-03
- Terminated
- 2017-04-12
- Reason
- Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
- Root cause
- Packaging
- Action
- Customed issued an "URGENT VOLUNTARY MEDICAL DEVICE RECALL" notification letter dated July 10, 2015 to all affected customers. The letter identified the product, problem, and actions to be taken by the customer.
- Quantity
- 507
- Distribution
- Distributed Only in Puerto Rico.
- Lot, serial or model codes
- Code:900403 Lots: 141015707 exp. 10/31/15 141216329 exp. 12/31/15 150116529 exp. 1/31/16 150116530 exp. 1/31/16 150116531 exp. 1/31/16 150116532 exp. 1/31/16 150317799 exp. 3/3/16 150317800 exp. 3/31/16 150317801 exp. 3/31/16 150317802 exp. 4/30/16 150418395 exp. 4/30/16 150418394 exp. 4/30/16 150418396 exp. 4/30/16 150518580 exp. 5/31/16 150518581 exp. 5/31/16
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- OHM
- Firm FEI
- 2648727
- Firm city
- Fajardo
- Firm state
- not on file
- Firm country
- PR
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28