Surgitube® 219Recalls & reported problems
Derma Sciences Canada Inc · 5/8 in X 50 yds Tubular Gauze, White · 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
- May 25, 2022Open, Classified
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.
Z-1799-2022 · Root cause: Environmental control · FDA record ↗
Other BANDAGE, ELASTIC devices
- Surgitube® 222Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 243Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 241Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 242Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 220Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- PROFORE KIT LATEX FREE 66020626Smith & Nephew Medical Limited · Bandage, Elastic45 reports
- PROFORE 18-25CM ANKLE CIRC. Case 8 66000016Smith & Nephew Medical Limited · Bandage, Elastic19 reports
- PROFORE LITE SYSTEM KIT Case 8 66000415Smith & Nephew Medical Limited · Bandage, Elastic14 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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