FDA Device recall Z-2543-2014

Zimmer PERSONA Distal Valgus Alignment Guide, Nonsterile. orthopedic surgical instrument

FDA Device
Class II
terminated
Published 2014-09-03

On 2014-09-03 the FDA classified a Class II recall of Zimmer PERSONA Distal Valgus Alignment Guide, Nonsterile. orthopedic surgical instrument by Zimmer, citing persona Distal Valgus Alignment guide collet locks are seizing in the 'unlocked' position.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2543-2014
Classification	Class II
Status	terminated
Initiated	2014-07-30
Published	2014-09-03
Last updated	2026-09-13 11:53 UTC
Company	Zimmer
Distribution	PR

Product

Zimmer PERSONA Distal Valgus Alignment Guide, Nonsterile. orthopedic surgical instrument. The device sets the proper Varus/Valgus alignment of a patient's knee prior to the initial femoral resection cut being made.

Reason

Persona Distal Valgus Alignment guide collet locks are seizing in the 'unlocked' position.

Identifiers

code_info	Item Number 42509900400, Lot Number: 62313324, 62415340, 62561031, 62668655, 62313326, 62430425, 62580270, 62695918,… Item Number 42509900400, Lot Number: 62313324, 62415340, 62561031, 62668655, 62313326, 62430425, 62580270, 62695918, 62341561, 62442314, 62590506, 62702686, 62358628, 62473246, 62594059, 62715932, 62368700, 62507846, 62611157, 62728374, 62376588, 62522771, 62624943, 62742362, 62396348, 62530133, 62637095, 62749057, 62401156, 62534170, 62641120, 62757397, 62407514, 62538842, 62662172, 62766074, 62410673, 62542958, & 62668654.

code_info

Item Number 42509900400, Lot Number: 62313324, 62415340, 62561031, 62668655, 62313326, 62430425, 62580270, 62695918,…

Item Number 42509900400, Lot Number: 62313324, 62415340, 62561031, 62668655, 62313326, 62430425, 62580270, 62695918, 62341561, 62442314, 62590506, 62702686, 62358628, 62473246, 62594059, 62715932, 62368700, 62507846, 62611157, 62728374, 62376588, 62522771, 62624943, 62742362, 62396348, 62530133, 62637095, 62749057, 62401156, 62534170, 62641120, 62757397, 62407514, 62538842, 62662172, 62766074, 62410673, 62542958, & 62668654.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2543-2014%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.