DELTA XTENDRecalls & reported problems across all models
Depuy (Ireland) · 194 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5,353
- Deaths reported
- 0
- Injuries reported
- 2,365
- Recalls
- 0
We found 194 models of DELTA XTEND by Depuy (Ireland) in the FDA's device registry (GUDID). Together they are named in 5,353 adverse event reports in the FDA's MAUDE database, received between Jun 23, 2017 and Sep 28, 2026 — classified as 2,365 injuries, 2,988 malfunctions.
The most frequently reported specific device problem is “Break” (1,435 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported DELTA XTEND problems
Device problems
- Break1,435
- Adverse Event Without Identified Device or Use Problem1,276
- Device Dislodged or Dislocated545
- Device-Device Incompatibility443
- Naturally Worn263
- Material Deformation218
- Osseointegration Problem200
- Material Twisted/Bent192
Patient problems
- No Clinical Signs, Symptoms or Conditions1,481
- No Consequences Or Impact To Patient931
- Unspecified Infection783
- No Code Available724
- Joint Dislocation474
- Pain416
- Insufficient Information292
- Inadequate Osseointegration287
DELTA XTEND models
194 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- DELTA XTEND 2307-92-003SCREWDRIVER751 reports
- DELTA XTEND 2307-95-000TEMPLATE315 reports
- DELTA XTEND 130760000shoulder prosthesis, reverse configuration223 reports
- DELTA XTEND 2307-74-002Orthopedic manual surgical instrument182 reports
- DELTA XTEND 130738203PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED175 reports
- DELTA XTEND 130790036PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED171 reports
- DELTA XTEND 130770018PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED159 reports
- DELTA XTEND 2307-93-000SCREWDRIVER154 reports
- DELTA XTEND 130760138PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DELTA XTEND 130790024PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED122 reports
- DELTA XTEND 130738206PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED116 reports
- DELTA XTEND 130760142PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED116 reports
- DELTA XTEND 2307-87-005IMPACTOR106 reports
- DELTA XTEND 130742203PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED104 reports
- DELTA XTEND 130742206PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED99 reports
- DELTA XTEND 130738209PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED87 reports
- DELTA XTEND 2307-87-003TEMPLATE86 reports
- DELTA XTEND 2307-74-101Orthopedic manual surgical instrument82 reports
- DELTA XTEND 2307-74-001Orthopedic manual surgical instrument80 reports
- DELTA XTEND 130760038PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED77 reports
- DELTA XTEND 130790042PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED72 reports
- DELTA XTEND 2307-89-000BIT, DRILL68 reports
- DELTA XTEND 130760042PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED66 reports
- DELTA XTEND 130730009PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED63 reports
- DELTA XTEND 2307-87-002IMPACTOR63 reports
- DELTA XTEND 2307-88-027REAMER60 reports
- DELTA XTEND 2307-90-005BIT, DRILL59 reports
- DELTA XTEND 2307-87-004ORTHOPEDIC MANUAL SURGICAL INSTRUMENT54 reports
- DELTA XTEND 2307-91-001GAUGE, DEPTH54 reports
- DELTA XTEND 130742209PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED52 reports
- DELTA XTEND 2307-83-000DRIVER, PROSTHESIS52 reports
- DELTA XTEND 2307-90-003shoulder prosthesis, reverse configuration43 reports
- DELTA XTEND 130712000shoulder prosthesis, reverse configuration36 reports
- DELTA XTEND 130770024PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED36 reports
- DELTA XTEND 130720103shoulder prosthesis, reverse configuration35 reports
- DELTA XTEND 130710000shoulder prosthesis, reverse configuration32 reports
- DELTA XTEND 130720101shoulder prosthesis, reverse configuration31 reports
- DELTA XTEND 130720102shoulder prosthesis, reverse configuration31 reports
- DELTA XTEND 1307-62-038PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED31 reports
- DELTA XTEND 130790048PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED30 reports
- DELTA XTEND 1307-61-142PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED27 reports
- DELTA XTEND 2307-67-000IMPACTOR26 reports
- DELTA XTEND 1307-62-142shoulder prosthesis, reverse configuration25 reports
- DELTA XTEND 2307-92-004SCREWDRIVER24 reports
- DELTA XTEND 130710100PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED23 reports
- DELTA XTEND 1307-64-138shoulder prosthesis, reverse configuration23 reports
- DELTA XTEND 130738106PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED21 reports
- DELTA XTEND 2307-38-403TEMPLATE21 reports
- DELTA XTEND 2307-60-138TEMPLATE21 reports
- DELTA XTEND 130720203shoulder prosthesis, reverse configuration20 reports
- DELTA XTEND 2307-60-142TEMPLATE20 reports
- DELTA XTEND 2307-88-242REAMER18 reports
- DELTA XTEND 1307-64-142shoulder prosthesis, reverse configuration17 reports
- DELTA XTEND 2307-71-000ORTHOPEDIC MANUAL SURGICAL INSTRUMENT16 reports
- DELTA XTEND 1307-61-138PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED16 reports
- Delta Xtend 1309-60-111PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED16 reports
- DELTA XTEND 1307-61-042PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED15 reports
- DELTA XTEND 130714000shoulder prosthesis, reverse configuration14 reports
- DELTA XTEND 2307-38-406TEMPLATE14 reports
- DELTA XTEND 2307-72-003TEMPLATE14 reports
- DELTA XTEND 1307-62-138PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED14 reports
- DELTA XTEND 130708100PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED13 reports
- DELTA XTEND 130742106PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED13 reports
- DELTA XTEND 2307-38-409TEMPLATE13 reports
- DELTA XTEND 140760020PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED12 reports
- DELTA XTEND 1307-64-038PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED12 reports
- DELTA XTEND 1307-61-038PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED12 reports
- DELTA XTEND 130770030PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED11 reports
- DELTA XTEND 2307-78-003REAMER11 reports
- DELTA XTEND 1307-20-113PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED11 reports
- DELTA XTEND 130720201shoulder prosthesis, reverse configuration10 reports
- DELTA XTEND 130770036PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED10 reports
- DELTA XTEND 2307-68-000IMPACTOR10 reports
- DELTA XTEND 2307-82-001TEMPLATE10 reports
- DELTA XTEND 130770042PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED9 reports
- DELTA XTEND 2307-42-403TEMPLATE9 reports
- DELTA XTEND 2307-60-038TEMPLATE9 reports
- DELTA XTEND 140760025PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED9 reports
- DELTA XTEND 1307-64-042shoulder prosthesis, reverse configuration9 reports
- DELTA XTEND 1307-66-142PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED9 reports
- DELTA XTEND 2307-84-000IMPACTOR9 reports
- DELTA XTEND 130720202shoulder prosthesis, reverse configuration8 reports
- DELTA XTEND 1307-62-042shoulder prosthesis, reverse configuration8 reports
- DELTA XTEND 1307-20-111PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED8 reports
- DELTA XTEND 2307-74-012TEMPLATE7 reports
- DELTA XTEND 2307-82-003REAMER7 reports
- DELTA XTEND 2307-86-002RETRACTOR7 reports
- DELTA XTEND 2307-99-002EXTRACTOR7 reports
- DELTA XTEND 1307-68-042shoulder prosthesis, reverse configuration7 reports
- DELTA XTEND 130748026PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED6 reports
- DELTA XTEND 2307-76-000REAMER6 reports
- DELTA XTEND 1407-60-010PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED6 reports
- DELTA XTEND 2317-70-024Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment6 reports
- DELTA XTEND 130748021PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED5 reports
- DELTA XTEND 2307-42-406TEMPLATE5 reports
- DELTA XTEND 2407-89-015BIT, DRILL5 reports
- DELTA XTEND 1307-66-038PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED5 reports
- DELTA XTEND 130752026PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED4 reports
- DELTA XTEND 2307-20-101TEMPLATE4 reports
Recent DELTA XTEND adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Unspecified Infection
MAUDE report 50923253 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Unspecified Infection
MAUDE report 50923234 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Unspecified Infection
MAUDE report 50923219 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Unspecified Infection
MAUDE report 50923207 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Unspecified Infection
MAUDE report 50923182 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Unspecified Infection
MAUDE report 50923063 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Unspecified Infection
MAUDE report 50923050 ↗InjurySep 25, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Joint Laxity
MAUDE report 50901801 ↗MalfunctionSep 25, 2026Difficult to Insert
It was reported that during an unknown surgery the Glenosphere could not be impacted onto the metaglene. There was no reported patient or user harm. There was no significant delay. The affected side was left. All available information has been disclosed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50897719 ↗InjurySep 24, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient presented with a painful right shoulder. The surgeon revised the glenosphere and poly.Affected Side: Unknown Shoulder.
Patient problems: Pain
MAUDE report 50881944 ↗InjurySep 24, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient presented with a painful right shoulder. The surgeon revised the glenosphere and poly.Affected Side: Unknown Shoulder.
Patient problems: Pain
MAUDE report 50881916 ↗MalfunctionSep 22, 2026Difficult to Insert
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50860060 ↗MalfunctionSep 22, 2026Difficult to Insert
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50860008 ↗MalfunctionSep 21, 2026Difficult to Insert
It was reported that intraoperatively it was not possible to fix both glenospheres in the metaglene. Another glenosphere and another metaglene were used, and the surgery was completed. The surgical delay was about 30 minutes. All available information has been disclosed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50841570 ↗MalfunctionSep 21, 2026Difficult to Insert
It was reported that intraoperatively it was not possible to fix both glenospheres in the metaglene. Another glenosphere and another metaglene were used, and the surgery was completed. The surgical delay was about 30 minutes. All available information has been disclosed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50841567 ↗
Other Depuy (Ireland) products
All Depuy (Ireland) devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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