V. Mueller SU2014-001Recalls & reported problems
Steris Corporation · V. Mueller UNIVERSAL BANDAGE SCISSORS BLACK PLASTIC HANDLES HEAVY-DUTY, AUTOCLAVABLE OVERALL LENGTH 7 inches 18CM · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names 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
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 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.
Recalls naming this device
- Nov 16, 2023Open, Classified
Bandage Scissors handle cover component contains an incorrect color masterbatch resin carrier. This may allow a pink dye/residue to appear on the Bandage Scissors and/or sterilization pouches after processing.
Z-0737-2024 · Root cause: Under Investigation by firm · FDA record ↗
Other SCISSORS, GENERAL, SURGICAL devices
- MEDLINE DYNJ04049Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls2 reports
- MEDLINE DYND04000Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls0 reports
- Centurion 66155Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall1 report
- Centurion I68790Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66150Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66350Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 67645Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66710Centurion 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
- 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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