CARDINAL HEALTH SEYHDCEDRERecalls & reported problems
Cardinal Health 200, LLC · STERILE DSC CULLOM EYE PACK · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10887488630205), received between Sep 23, 2020 and Sep 23, 2020 — classified as 3 injuries.
The most frequently reported specific device problem is “Contamination” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available2
- Contamination1
Patient problems
- Toxic Anterior Segment Syndrome (TASS)3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjurySep 23, 2020Appropriate Device Problem Term/Code Not Available
CUSTOMER REPORTED THAT DURING A CATARACT EXTRACTION WITH INTRAOCULAR LENS IMPLANT PROCEDURE, THE MAYO STAND COVER A8337CN FROM EYE PACK SEYHDCEDRE WAS FOUND TO HAVE A FUZZY LAYER AFTER MOVING INSTRUMENTS AROUND SO A TOWEL WAS PLACED OVER THE MAYO COVER. THERE WAS NO DELAY. THE PATIENT DEVELOPED INFLAMMATION OF THE LEFT EYE AND POSSIBLE TASS SO CUSTOMER IS LOOKING INTO ALL POSSIBLE CAUSES. THE PRESCRIBED ROUTINE MEDICATION PREDNISOLONE WAS ORDERED TO BE GIVEN PUNCTA OCCLUSION DUE TO THE INFLAMMATION. NO NEW MEDICATIONS WERE ORDERED DUE TO THE INFLAMMATION.
Patient problems: Toxic Anterior Segment Syndrome (TASS)
MAUDE report 10577570 ↗InjurySep 23, 2020Contamination
CUSTOMER REPORTED THAT DURING A CATARACT EXTRACTION WITH INTRAOCULAR LENS IMPLANT PROCEDURE, THE MAYO STAND COVER (B)(6) FROM EYE PACK SEYHDCEDRE WAS FOUND TO HAVE A FUZZY LAYER AFTER MOVING INSTRUMENTS AROUND SO A TOWEL WAS PLACED OVER THE MAYO COVER. THERE WAS NO DELAY. THE PATIENT DEVELOPED MILD EXCESS INFLAMMATION OF THE LEFT EYE WITH POSSIBLE TASS SO CUSTOMER IS LOOKING INTO ALL POSSIBLE CAUSES. THE FREQUENCY OF ADMINISTRATION OF THE ROUTINE PREDNISOLONE WAS CHANGED FROM EVERY 4 HOURS TO EVERY 2 HRS FOR ONE DAY POST INFLAMMATION. NO NEW MEDICATIONS WERE ORDERED DUE TO THE INFLAMMATION.
Patient problems: Toxic Anterior Segment Syndrome (TASS)
MAUDE report 10577526 ↗InjurySep 23, 2020Appropriate Device Problem Term/Code Not Available
CUSTOMER REPORTED THAT DURING A CATARACT EXTRACTION WITH INTRAOCULAR LENS IMPLANT PROCEDURE, THE MAYO STAND COVER A8337CN FROM EYE PACK SEYHDCEDRE WAS FOUND TO HAVE A FUZZY LAYER AFTER MOVING INSTRUMENTS AROUND SO A TOWEL WAS PLACED OVER THE MAYO COVER. THERE WAS NO DELAY. THE PATIENT DEVELOPED TOXIC ANTERIOR SEGMENT SYNDROME TASS SO CUSTOMER IS LOOKING INTO ALL POSSIBLE CAUSES. DUROZEL EYE DROPS WERE PRESCRIBED TO TREAT THE TASS.
Patient problems: Toxic Anterior Segment Syndrome (TASS)
MAUDE report 10577284 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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