Skip to the content

FDA Medical Device Recalls (openFDA)

Corin Ltd: TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.

Recall number
Z-1667-2022
Recalling firm
Corin Ltd
Product
TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.
Status
Terminated
Initiated
2022-07-12
Posted
not on file
Terminated
2026-05-04
Reason
Some of the devices did not pass fatigue testing.
Root cause
Under Investigation by firm
Action
The recalling firm issued the recall letter dated 7/8/2022 via email to the consignee on 7/12/2022. The recall letter described the potential issue and listed the affected product. The potential risk was reported and the actions to be carried out by the customer, which included return of the product from the field and completion of the acknowledgement form to be returned via email to confirm receipt of the letter.
Quantity
1
Distribution
Distribution was made to NJ. There was no military/government distribution.
Lot, serial or model codes
Model #588.3800, Lot #494754; UDI 05055343871065
510(k) numbers
["K142761"]
PMA numbers
not on file
Product code
JDI
Firm FEI
3002806725
Firm city
Cirencester
Firm state
not on file
Firm country
United Kingdom

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

Search this register