FDA Device recall Z-2156-2024

OPTETRAK One Peg Patella,, Item Numbers: a) 200-03-26, 26MM

FDA Device
Class II
ongoing
Published 2024-06-26

On 2024-06-26 the FDA classified a Class II recall of OPTETRAK One Peg Patella,, Item Numbers: a) 200-03-26, 26MM by Exactech, citing exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2156-2024
Classification	Class II
Status	ongoing
Initiated	2024-04-18
Published	2024-06-26
Last updated	2026-09-13 11:57 UTC
Company	Exactech
Distribution	n/a

Product

OPTETRAK One Peg Patella,, Item Numbers: a) 200-03-26, 26MM; b) 200-03-29, 29MM; c) 200-03-32, 32MM; d) 200-03-35, 35MM; e) 200-03-38, 38MM; f) 200-03-41, 41MM

Reason

Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.

Identifiers

code_info	a) 200-03-26, UDI/DI 10885862039637, Lot Numbers: 6389536, 6389549, 6389551, 6389538, 6389540, 6389531, 6389537, 63895… a) 200-03-26, UDI/DI 10885862039637, Lot Numbers: 6389536, 6389549, 6389551, 6389538, 6389540, 6389531, 6389537, 6389529, 6389534, 6389542, 6389545, 6711546, 6711550, 6389547, 6389548, 6389555, 6711540; b) 200-03-29, UDI/DI 10885862039644, Lot Numbers: 6276447, 6276452, 6385318, 6385319, 6607740, 6385323, 6385304, 6385321, 6276446, 6276448, 6385300, 6276442, 6385310, 6385316, 6385325, 6607741, 7037109, 6276425, 6276429, 6276428, 6276433, 6276450, 6276453, 6607760, 6276437, 6276440, 6607751, 6607754, 6276426, 6276445, 6276449, 6607744, 6607759, 6276434, 6276435, 6276443, 6276451, 6385307; c) 200-03-32, UDI/DI 10885862039651, Lot Numbers: 6385285, 6385286, 6844803, 6844831, 6385268, 6385278, 7043349, 7043358, 7043331, 6844822, 6385266, 6385269, 6385272, 6385277, 6385274, 7043330, 7043333, 7043336, 7043337, 7043342, 7043343, 7043356, 6385273, 6385281, 6385294, 6844804, 6844817, 6844818, 6844826; d) 200-03-35, UDI/DI 10885862039668, Lot Numbers: 6711235, 6711254, 7044342, 7044351

code_info

a) 200-03-26, UDI/DI 10885862039637, Lot Numbers: 6389536, 6389549, 6389551, 6389538, 6389540, 6389531, 6389537, 63895…

a) 200-03-26, UDI/DI 10885862039637, Lot Numbers: 6389536, 6389549, 6389551, 6389538, 6389540, 6389531, 6389537, 6389529, 6389534, 6389542, 6389545, 6711546, 6711550, 6389547, 6389548, 6389555, 6711540; b) 200-03-29, UDI/DI 10885862039644, Lot Numbers: 6276447, 6276452, 6385318, 6385319, 6607740, 6385323, 6385304, 6385321, 6276446, 6276448, 6385300, 6276442, 6385310, 6385316, 6385325, 6607741, 7037109, 6276425, 6276429, 6276428, 6276433, 6276450, 6276453, 6607760, 6276437, 6276440, 6607751, 6607754, 6276426, 6276445, 6276449, 6607744, 6607759, 6276434, 6276435, 6276443, 6276451, 6385307; c) 200-03-32, UDI/DI 10885862039651, Lot Numbers: 6385285, 6385286, 6844803, 6844831, 6385268, 6385278, 7043349, 7043358, 7043331, 6844822, 6385266, 6385269, 6385272, 6385277, 6385274, 7043330, 7043333, 7043336, 7043337, 7043342, 7043343, 7043356, 6385273, 6385281, 6385294, 6844804, 6844817, 6844818, 6844826; d) 200-03-35, UDI/DI 10885862039668, Lot Numbers: 6711235, 6711254, 7044342, 7044351

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-2156-2024%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.