MEDLINE DYND04000Recalls & reported problems
Medline Industries, Inc. · O.R. SCISSORS, S/B, 5.5 STERILE · Class 1
Data updated Oct 16, 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
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 3
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Nov 13, 2025Open, Classified
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Z-0921-2026 · Root cause: Packaging process control · Recall details · FDA record ↗
- Nov 12, 2024Open, Classified
Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.
Z-0755-2025 · Root cause: Process control · Recall details · FDA record ↗
- Feb 23, 2024Open, Classified
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Z-1444-2024 · Root cause: Process control · Recall details · FDA record ↗
Other SCISSORS, GENERAL, SURGICAL devices
- MEDLINE DYNJ04049Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls2 reports
- Centurion 66155Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall1 report
- Sklar Instruments 96-2673ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2266Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2502Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion TRI67630Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2492ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2531ASklar 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 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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