FDA Class II · Medical device · July 1, 2026
Acumed Hexalob Screw various sizes recall — Acumed LLC
Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.
Official ID Z-2532-2026 · Official record ↗
Acumed recalls
Recall found. Acumed is named in FDA Class II recall Z-2532-2026 covering Acumed Hexalob Screw various sizes. Hazard: Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use. Identifying details: 3070-27008/Lots: 668261/UDI: 10806378125997; 3070-27009/Lots: 680797/UDI: 10806378126000; 3070-27010/Lots: 667231, 682194/UDI: 10806378126017; 3070-27011/Lots: 680621, 680737/UDI: 10806378126024; 3070-27012/Lots: 667233, 668266, 668704, 682195/UDI: 10806378126031; 3070-27013/Lots:668706, 680400/UDI: 10806378126048; 3070-27014/Lots: 667236, 668705, 680935/UDI: 10806378126055; 3070-27015/Lots: 667237, 680936/UDI: 10806378126062; 3070-27016/Lots: 668269, 682390/UDI: 10806378126079; 3070-27017/Lot: 681575/UDI: 10806378126086; 3070-27018/Lot: 667169, 668260, 682482/UDI: 10806378126093; 3076-30010/Lots: 667202, 668271/UDI: 10806378126109; 3076-30012/Lots: 667242, 668273/UDI: 10806378126116; 3076-30014/Lots: 667205, 668272/UDI: 10806378126123. Status: Ongoing.
Models with recalls
All Acumed recalls
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.