FDA Device recall Z-1328-2023
Medtronic Grafton Matrix Strips: a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS, REF S42275
- FDA Device
- Class II
- ongoing
- Published 2023-04-12
On 2023-04-12 the FDA classified a Class II recall of Medtronic Grafton Matrix Strips: a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS, REF S42275 by Medtronic Sofamor Danek Usa, citing potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1328-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-08 |
| Published | 2023-04-12 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Sofamor Danek Usa |
| Distribution | US |
Product
Medtronic Grafton Matrix Strips: a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS, REF S42275; b) DBM S42280 8MMX1CMX20CM 2EA MATRX STRPS, REF S42280; c) DBM T42275 8MMX1CMX10CM 2 EACH GRAFTON M, REF T42275; d) DBM T42275AUS 8MMX1CMX10CM 2 EA GRFTON S, REF T42275AUS; e) DBM T42275INT 8MMX1CMX10CM 2 EA GRFTON S, REF T42275INT; f) DBM T42275JPN GRAFTON MATRIX 1CM X 10CM, REF T42275JPN; g) DBM T42280 8MMX1CMX20CM 2 EACH GRAFTON M, REF T42280; h) DBM T42280AUS 8MMX1CMX20CM 2 EA GRFTON S, REF T42280AUS; i) DBM T42280INT 8MMX1CMX20CM 2 EA GRFTON S, REF T42280INT; j) DBM T42280JPN GRAFTON MATRIX 1CM X 20CM, REF T42280JPN; Demineralized Bone Matrix (DBM) product
Reason
Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.
Identifiers
| code_info | a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS, REF S42275, GTIN 00613994960931, Serial Numbers: A42914, A43126, A43182,…a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS, REF S42275, GTIN 00613994960931, Serial Numbers: A42914, A43126, A43182, A43185, A43460, A43613, A43715, A43896, A44262, A44388, A44561, A45997, A46401, A46690, A46699, A47001, A47719, A47942, A48136, A48371, A48792, A49045, A49089, A49108, A49790, A49952, A50039, A50528, A50688, A51827, A52539, A52601, A52788, A53401, A53671, A53788, A53881, A53904, A54204, A54988, A55032, A55132; b) DBM S42280 8MMX1CMX20CM 2EA MATRX STRPS, REF S42280, GTIN 00613994960924, Serial Numbers: A42850, A43731, A44343, A44529, A44821, A45022, A45035, A46734, A47604, A47621, A47701, A47971, A48051, A48578, A49616, A51011, A52580, A52809, A54208, A54369, A54440, A54597, A55584; c) DBM T42275 8MMX1CMX10CM 2 EACH GRAFTON M, REF T42275, GTIN 00643169123076, Serial Numbers: A39563-061, A39563-062, A39563-063, A39563-064, A39563-065, A39563-066, A39563-068, A39563-070, A39563-071, A39563-072, A39563-073, A39563-074, A39563-075, A39563-076, A39563-077, A40837-011, |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1328-2023%22
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