MEDLINE DYNJ04049Recalls & reported problems
Medline Industries, Inc. · SCISSORS,IRIS,CURVED,STD,4.5',STERILE · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
3 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 3
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196847273), received between Sep 9, 2026 and Sep 17, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).
3 FDA recall records name this device's identifier, 3 still open.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Oct 21, 2024Open, Classified
Tip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility.
Z-0465-2025 · Root cause: Under Investigation by firm · FDA record ↗
- Apr 30, 2024Open, Classified
There is the potential of the tip protector to fall off 4.5" sterile, curved, Iris Scissors
Z-2024-2024 · Root cause: Under Investigation by firm · FDA record ↗
- Aug 3, 2023Open, Classified
4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to the potential of the tip protector to fall off. The sharp tip of the scissors could compromise the sterile barrier system by puncturing large and/or small holes that may not be visible to the user.
Z-2595-2023 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Detachment of Device or Device Component2
- Device Misassembled During Manufacturing /Shipping1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Detachment of Device or Device Component
It was reported that "the tip protector off in the packaging of only 1 pair of scissors."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50803352 ↗MalfunctionSep 9, 2026Detachment of Device or Device Component; Device Misassembled During Manufacturing /Shipping
It was reported that the scissor cap is falling off of the scissors causing the sharp tip to puncture the packaging and potentially cause harm to providers.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50690272 ↗
Other SCISSORS, GENERAL, SURGICAL devices
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- Centurion 66710Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 67450Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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