FDA Device Intelligence
HomeDevice types › JDS

Nail, Fixation, Bone

FDA product code JDS · Class 2 · Orthopedic

7,967
Registered devices
7,230
Adverse events
21
Recalls
53
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-09-26Synthes (USA) Products LLCAlthough the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged and labele
2025-09-26Synthes (USA) Products LLCAlthough the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged and labele
2022-04-22Smith & Nephew Orthopaedics GmbHRight nails were anodized, marked, and labelled as left nails and vice versa
2020-11-02Smith & Nephew, Inc.Manufacturing packaging error.
2020-06-24Smith & Nephew, Inc.A manufacturing error which resulted in the re-sterilization of the ultra-high-molecular-weight polyethylene (UHMWPE) sleeve.
2017-10-24Smith & Nephew, Inc.A single lot of INTERTAN 10S 10 MM X 18 CM 130 D was manufactured with the screw inserted upside down.
2017-02-17Zimmer Biomet, Inc.Endotoxin levels higher than process maximum limits were discovered in the identified polyethylene components.
2015-06-03Synthes, Inc.A specific part and lot number was packaged and shipped prior to the completion of a required internal inspection.
2014-07-02Smith & Nephew, Inc.There was an error in manufacturing which resulted in the proximal lag screw hole being positioned incorrectly in several batches of TRIGEN(R); INTERTAN(TM); NA
2014-04-04Smith & Nephew IncA manufacturing error resulted in the set screw being inserted too deep in the affected nails.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.