OMNISPAN ORTHOCORDRecalls & reported problems across all models
Medos International Sàrl · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,581
- Deaths reported
- 0
- Injuries reported
- 26
- Recalls
- 0
We found 3 models of OMNISPAN ORTHOCORD by Medos International Sàrl in the FDA's device registry (GUDID). Together they are named in 1,581 adverse event reports in the FDA's MAUDE database, received between Feb 15, 2018 and Sep 30, 2026 — classified as 26 injuries, 1,555 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (529 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 OMNISPAN ORTHOCORD problems
Device problems
- Device-Device Incompatibility529
- Premature Activation360
- Break171
- Positioning Failure104
- Migration99
- Difficult to Advance77
- Detachment of Device or Device Component69
- Activation, Positioning or Separation Problem48
Patient problems
- No Clinical Signs, Symptoms or Conditions1,164
- No Consequences Or Impact To Patient371
- Not Applicable19
- No Known Impact Or Consequence To Patient17
- No Code Available16
- Tissue Damage14
- Foreign Body In Patient5
- Unspecified Tissue Injury4
OMNISPAN ORTHOCORD models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- OMNISPAN ORTHOCORD 228142FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE932 reports
- OMNISPAN ORTHOCORD 228141FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE609 reports
- OMNISPAN ORTHOCORD 228140FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE40 reports
Recent OMNISPAN ORTHOCORD adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952189 ↗MalfunctionSep 30, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952181 ↗MalfunctionSep 30, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952179 ↗MalfunctionSep 30, 2026Device-Device Incompatibility
It was reported that during an arthroscopic meniscal repair procedure the OMNISPAN MENISCAL REPAIR 27DEG device could not fire (deploy). Another device was used to complete the procedure. There was no delay in the procedure reported. There were no adverse patient consequences reported. All available information has been disclosed. This is report 2 of 3 for (b)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951660 ↗MalfunctionSep 29, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938086 ↗MalfunctionSep 29, 2026Difficult to Advance
It was reported that during a meniscal repair surgical procedure, while using the OMNISPAN MENISCAL REPAIR 27DEG anchor device, it was observed that the 2nd plate could not fix the meniscus after deployment. It was reported that another device was used to complete the surgery. There were no adverse consequences to the patient. No additional information could be provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935983 ↗MalfunctionSep 29, 2026Break
It was reported that during a cruciate ligament repair surgical procedure, when using the OMNISPAN MENISCAL REPAIR 12DEG anchor device it was observed that the needle was broken off. It was reported that another device was used to complete the surgery. There were no adverse consequences to the patient. No additional information could be provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935541 ↗MalfunctionSep 29, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935391 ↗MalfunctionSep 29, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934548 ↗MalfunctionSep 29, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934533 ↗MalfunctionSep 29, 2026Premature Activation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50930121 ↗MalfunctionSep 28, 2026Nonstandard Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923796 ↗MalfunctionSep 28, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50921685 ↗MalfunctionSep 28, 2026Difficult to Advance
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50921652 ↗MalfunctionSep 28, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50920410 ↗
Other Medos International Sàrl products
- TRUESPAN ORTHOCORD6 models · 4,109 reports
- FMS39 models · 3,588 reports
- EXPEDIUM291 models · 3,312 reports
- EXPEDIUM VERSE90 models · 2,686 reports
- EXPRESSEW6 models · 2,459 reports
- HEALIX ADVANCE ORTHOCORD21 models · 1,311 reports
- PROWLER SELECT9 models · 1,066 reports
- GRYPHON ORTHOCORD6 models · 918 reports
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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