FDA Medical Device Recalls (openFDA)
ROi CPS LLC: Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.
- Recall number
- Z-1408-2022
- Recalling firm
- ROi CPS LLC
- Product
- Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.
- Status
- Terminated
- Initiated
- 2022-06-03
- Posted
- 2022-07-19
- Terminated
- 2023-04-14
- Reason
- Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.
- Root cause
- Process change control
- Action
- The recalling firm initiated the recall via telephone on 6/3/2022 to the direct consignee of Item 830019017, explained the reason for recall, and instructed the product be quarantined. The recalling firm also contacted the end user who had received distribution from the direct consignee. The end user was informed of the error and was requested to remove the affected lot from their inventory. The recalling firm worked with the end user to have the kits returned to the direct consignee where they were placed in quarantine. Regarding the recall of Item #830099008 and Item #830014016, the direct consignees were notified on 6/6/2022 via telephone requesting the affected kits be placed on hold and moved to a quarantined area. A follow-up email was sent to the recall coordinator for the direct consignees (which was the same recall coordinator) on 6/16/2022 which contained a correction notice. The email explained the issue and said the recalling firm has already performed rework on the kits in the inventory at their location (the two direct consignee locations) so no additional actions were required except for the completion of the reply form to indicate receipt of the notice. The attached Medical Device Correction Notice was dated 6/16/2022 and explained the issue, the affected product, the health risk assessment, and the actions taken by the recalling firm, which included rework of the products that had been returned to the direct consignees. The enclosed replay form was to be completed acknowledging the consignee has read and understands the notice.
- Quantity
- 40 kits
- Distribution
- Distribution was made to MO. There was no foreign/military/government distribution.
- Lot, serial or model codes
- Lot #92605, exp. 8/31/2023, Item #830014016, UDI #10194717110156.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- OHM
- Firm FEI
- 3014527682
- Firm city
- Republic
- 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