RecallRadar

FDA Device recall Z-1713-2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile- Indicated for temporary in…

On 2024-05-08 the FDA classified a Class II recall of ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile- Indicated for temporary in… by Zimmer, citing thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user sin….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1713-2024
ClassificationClass II
Statusongoing
Initiated2024-03-20
Published2024-05-08
Last updated2026-09-13 11:57 UTC
CompanyZimmer
DistributionUS

Product

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-12

Reason

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Identifiers

code_info
UDI: (01)00889024088535(17)290809(10)64475610 (01)00889024088535(17)310331(10)65038408 (01)00889024088535(17)310324(10…UDI: (01)00889024088535(17)290809(10)64475610 (01)00889024088535(17)310331(10)65038408 (01)00889024088535(17)310324(10)65038409 (01)00889024088535(17)310915(10)65209412 (01)00889024088535(17)310915(10)65209413 Lot Numbers: 64475610 65038408 65038409 65209412 65209413

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1713-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.