Sage AirTAP LC 7289Recalls & reported problems
Sage Products, LLC · Sage AirTAP LC 10 Pack Configuration · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00618029720856), received between Dec 23, 2024 and Dec 23, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
- Use of Device Problem1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 23, 2024Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information
REPORT RECEIVED OF A PATIENT INJURY. REPORTER STATED A PATIENT FELL WHILE THE AIRTAP LC DEVICE WAS IN USE. REPORTER STATED ON APPROXIMATELY (B)(6) 2024 THE DEVICE WAS BEING USED FOR A TRANSFER FROM THE INTERVENTIONAL RADIOLOGY TABLE TO A TRANSFER CART. REPORTER STATED THE DEVICE WAS NOT BEING USED WITH A LIFT BUT WAS INFLATED TO ASSIST IN THE TRANSFER. REPORTER STATED THE DEVICE INFLATED CORRECTLY AND DID NOT MALFUNCTION. REPORTER STATED THE PATIENT WAS CENTERED ON THE DEVICE BUT OFF CENTERED ON THE TABLE AND WHEN THE DEVICE WAS INFLATED THE PATIENT FELL OFF THE SIDE OF THE TABLE. THE REPORTER STATED THERE ARE NO SIDE RAILS ON THE BED. STAFF WERE PRESENT ON THE SIDE OF THE RECEIVING SURFACE; HOWEVER, NO STAFF WERE PRESENT ON THE SIDE OF THE SENDING SURFACE WHICH WAS THE SIDE FROM WHICH THE PATIENT FELL. REPORTER STATED THE FALL RESULTED IN AN UNSPECIFIED INJURY THAT REQUIRED HOSPITALIZATION. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: Fall
MAUDE report 21005310 ↗
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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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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