FDA Device recall Z-1437-2014
GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # 2230-00-019, Non-Sterile, DePuy, Johnson & Johnson Product Usage: U…
- FDA Device
- Class II
- terminated
- Published 2014-04-16
On 2014-04-16 the FDA classified a Class II recall of GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # 2230-00-019, Non-Sterile, DePuy, Johnson & Johnson Product Usage: U… by Depuy Orthopaedics, citing urgent Device Correction notifications are being sent to USA distributors with follow-up to surgeons concerning updated surgical techniques stressing the possibility of the should….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1437-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-28 |
| Published | 2014-04-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Depuy Orthopaedics |
| Distribution | US |
Product
GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # 2230-00-019, Non-Sterile, DePuy, Johnson & Johnson Product Usage: Usage: The GLOBAL APG+ 2.5mm Guide Pin is a single-use instrument that is used to assist the surgeon in the orientation of the cannulated reamer(s) and cannulated central drills in the preparation of the glenoid surface. The GLOBAL APG+ 2.5mm Guide Pin is validated for use with the GLOBAL APG+, GLOBAL STEPTECH APG, and DELTA XTEND Systems. The guide pin is scored in three locations, which allows the surgeon to select a desired pin length. The single-use shoulder instrument is made from 316L Stainless Steel.
Reason
Urgent Device Correction notifications are being sent to USA distributors with follow-up to surgeons concerning updated surgical techniques stressing the possibility of the shoulder pin guide breaking and potentially being left in the patient.
Identifiers
| code_info | Label Lot Laser Lot D38FX4 PG0809 D5AA34 PG1009 D5AA44 PG1109 E1WC14 PG0710 E1WC24 PG0710 E1WC34 PG0810 E1WC…Label Lot Laser Lot D38FX4 PG0809 D5AA34 PG1009 D5AA44 PG1109 E1WC14 PG0710 E1WC24 PG0710 E1WC34 PG0810 E1WC44 PG0810 E1WCY4 PG0710 E24A44 PG0810 E24A54 PG0810 E28CB4 PG0810 E29G14 PG1210 E2FCW4 PG0810 E2FCX4 PG0810 E2FCY4 PG0810 E2VB24 PG0910 E2VB34 PG0810 E2VB44 PG0810 E2VB54 PG0910 E2VB64 PG0910 E2VB74 PG1010 E41E44 PG1010 E41E54 PG1010 E4DA54 PG0910 E4FDM4 PG0910 E4FDN4 PG1110 E4FDP4 PG0910 E4FKJ4 PG1010 E4FKK4 PG1110 E4FKL4 PG1010 E4XFD4 PG0910 E4XFE4 PG0910 E4XGL4 PG1010 E4XGM4 PG1010 E4XGN4 PG1010 E4XGR4 PG1010 E4XGS4 PG1010 E4XGT4 PG1010 E54BL4 PG1110 E54BP4 PG1110 E56JF4 PG1210 E56JG4 PG1210 E57F14 PG1210 E57F24 PG1210 E57F34 PG1210 E57F44 PG1110 E57FV4 PG1110 E57FW4 PG1110 E57FY4 PG1210 E5CCG4 PG1010 E5CCH4 PG1010 E5CCJ4 PG1010 E5CCK4 PG1010 E5NJV4 PG1110 E5PBJ4 PG1210 E5PEA4 PG1110 E6CHE4 PG1110 E6DDE4 PG1210 E6DDF4 PG1210 E75AK4 PG1210 E75AL4 PG1210 E87GG4 PG1210 E87GH4 PG0111 E87GJ4 PG0111 E87GK4 PG1210 |
|---|
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-1437-2014%22
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