MONOCRYLRecalls & reported problems across all models
Ethicon, LLC · 127 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
MONOCRYL models — page 2
127 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- MONOCRYL Y835GSUTURE, ABSORBABLE, SYNTHETIC3 reports
- MONOCRYL Y942HSUTURE, ABSORBABLE, SYNTHETIC3 reports
- MONOCRYL YB257SUTURE, ABSORBABLE, SYNTHETIC3 reports
- MONOCRYL D8955SUTURE, ABSORBABLE, SYNTHETIC2 reports
- MONOCRYL MCP214HSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID2 reports
- MONOCRYL MCP495GSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID2 reports
- MONOCRYL MCP823GSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID2 reports
- MONOCRYL Y219HSUTURE, ABSORBABLE, SYNTHETIC2 reports
- MONOCRYL Y513GSUTURE, ABSORBABLE, SYNTHETIC2 reports
- MONOCRYL Y682HSUTURE, ABSORBABLE, SYNTHETIC2 reports
- MONOCRYL Y822GSUTURE, ABSORBABLE, SYNTHETIC2 reports
- MONOCRYL Y834GSUTURE, ABSORBABLE, SYNTHETIC2 reports
- MONOCRYL Y844GSUTURE, ABSORBABLE, SYNTHETIC2 reports
- MONOCRYL Y771DSuture, absorbable, synthetic, polyglycolic acid2 reports
- MONOCRYL D8762SUTURE, ABSORBABLE, SYNTHETIC1 report
- MONOCRYL D8901SUTURE, ABSORBABLE, SYNTHETIC1 report
- MONOCRYL D9503SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- MONOCRYL MCP213HSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- MONOCRYL MCP605HSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- MONOCRYL MCP923HSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- MONOCRYL MCP944HSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- MONOCRYL MCPB944HSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- MONOCRYL Y357HSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- MONOCRYL Y492GSUTURE, ABSORBABLE, SYNTHETIC1 report
- MONOCRYL Y814GSUTURE, ABSORBABLE, SYNTHETIC1 report
- MONOCRYL Y917HSUTURE, ABSORBABLE, SYNTHETIC1 report
- MONOCRYL YB416SUTURE, ABSORBABLE, SYNTHETIC1 report
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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