Sage Air Tap LC 7287Recalls & reported problems
Sage Products, LLC · Sage Air Tap Lift Compatible · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00618029720801), received between Sep 22, 2021 and Oct 21, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (3 reports).
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.
Most reported problems
Device problems
- Material Split, Cut or Torn3
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 21, 2022Material Split, Cut or Torn; Material Split, Cut or Torn
REPORT RECEIVED OF A STRAP THAT BROKE ON THE SAGE AIRTAP LC DEVICE WHILE IT WAS BEING USED TO TRANSFER A DECEASED PATIENT TO A CART IN ORDER TO BE TRANSFERRED TO THE MORGUE. ALTHOUGH SEVERAL ATTEMPTS WERE MADE, COMPANY SALES REPRESENTATIVE WAS UNABLE TO GAIN ANY ADDITIONAL INFORMATION. NO LOT INFORMATION, PRODUCT OR PHOTOGRAPHS WERE PROVIDED.
Patient problems: Insufficient Information
MAUDE report 15654240 ↗MalfunctionSep 22, 2021Material Split, Cut or Torn; Material Split, Cut or Torn
REPORT RECEIVED OF A STRAP RIPPING ON THE SAGE AIRTAP LC DEVICE. IT IS UNKNOWN WHETHER THERE WAS PATIENT INVOLVEMENT OR ANY PATIENT OR STAFF INJURY. SEVERAL ATTEMPTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION; HOWEVER THE REPORTER DID NOT RESPOND. NO LOT INFORMATION, PRODUCT OR PHOTOGRAPHS WERE PROVIDED. ALTHOUGH REQUESTED, NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12515724 ↗MalfunctionSep 22, 2021Material Split, Cut or Torn; Material Split, Cut or Torn
REPORT RECEIVED OF A STRAP RIPPING ON THE SAGE AIRTAP LC DEVICE WHILE HOOKED UP TO A (B)(6) PATIENT. REPORTER WAS UNABLE TO PROVIDE ANY ADDITIONAL INFORMATION. NO LOT INFORMATION, PRODUCT OR PHOTOGRAPHS WERE PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12515033 ↗
Other Protector, skin pressure devices
- Arthrex AR-1650-01Allen Medical Systems, Inc. · Protector, skin pressure2 reports
- Arthrex® AR-1650-02Arthrex, Inc. · Protector, skin pressure1 report
- Gel Corn Pads, Black, One Size, Bulk 31705Silipos Holding LLC · Protector, Skin Pressure1 report
- Mölnlycke® Z-Flex™ Fluidized Heel Boot 1400123Mölnlycke Health Care AB · Protector, skin pressure1 report
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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