Aspira Dressing Kit 4991503Recalls & reported problems
Bard Access Systems, Inc. · Aspira Dressing Kit · Class 2 · Implant
Data updated Oct 16, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.
Z-1599-2022 · Root cause: Environmental control · Recall details · FDA record ↗
Other APPARATUS, SUCTION, PATIENT CARE devices
- PleurX 50-7050Carefusion 2200, Inc · APPARATUS, SUCTION, PATIENT CARE137 reports
- PleurX 50-7500BCarefusion 2200, Inc · Apparatus, Suction, Patient Care66 reports
- Aspira® 00884450394946Merit Medical Systems, Inc. · APPARATUS, SUCTION, PATIENT CARE1 recall2 reports
- Aspira® 00884450394915Merit Medical Systems, Inc. · APPARATUS, SUCTION, PATIENT CARE1 recall2 reports
- Aspira® 00884450394861Merit Medical Systems, Inc. · APPARATUS, SUCTION, PATIENT CARE1 recall1 report
- Aspira® 00884450398173Merit Medical Systems, Inc. · APPARATUS, SUCTION, PATIENT CARE1 recall0 reports
- Aspira® 00884450394939Merit Medical Systems, Inc. · APPARATUS, SUCTION, PATIENT CARE1 recall0 reports
- Aspira® 00884450394960Merit Medical Systems, Inc. · APPARATUS, SUCTION, PATIENT CARE1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page