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FDA Medical Device Recalls (openFDA)

Resource Optimization & Innovation Llc: Regard Custom Surgical Pack, Item Number: 800208002; Sterile, CV0361B - CABG A&B. Used in cardiovascular surgical procedures.

Recall number
Z-2799-2015
Recalling firm
Resource Optimization & Innovation Llc
Product
Regard Custom Surgical Pack, Item Number: 800208002; Sterile, CV0361B - CABG A&B. Used in cardiovascular surgical procedures.
Status
Terminated
Initiated
2015-08-19
Posted
2015-09-21
Terminated
2017-04-05
Reason
Surgical kits contain a surgical scrub product which may be chemically contaminated and lack sterility assurance.
Root cause
Material/Component Contamination
Action
On 8/19/2015, the recalling firm sent its two consignees an email with the recall notice attached. The notice notified their customers that they were affected by the recalling firm's supplier's recall. The notice instructed the customers to dispose of the recalled component and acknowledge receipt of the recall notice.
Quantity
67 kits
Distribution
Distributed to one customer in Lake Charles, LA and one customer in Spartanburg, SC.
Lot, serial or model codes
025072B
510(k) numbers
not on file
PMA numbers
not on file
Product code
LRO
Firm FEI
3004513970
Firm city
Springfield
Firm state
MO
Firm country
not on file

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
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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

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