MaxonRecalls & reported problems across all models
Covidien LP · 114 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Maxon models — page 2
114 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Maxon 8886614921-2SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886621721-2SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon X1394SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6007-41SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6036-41SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6061-63SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6257-61SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6269-51SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6419-71SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6612-31SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon 8886 6755-71SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon GMMT-951SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon GMMT-961SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 report
- Maxon XX-2108SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 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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