PIGGYBACK IPN913628Recalls & reported problems
Teleflex Incorporated · Piggyback 145cm · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841156101657), received between Jun 10, 2020 and Jun 10, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 10, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
REPORTED AS MARKER BAND CAME OFF THE PIGGYBACK. MEDWATCH UF/IMPORTER# (B)(4) WAS RECEIVED 15MAY2020. THE DESCRIPTION FROM THE MEDWATCH STATES: RADIOPAQUE MARKER BROKE OFF CATHETER WHILE INSIDE PATIENT. DEVICE FAILED (E.G., BROKE COULDN'T GET IT TO WORK OR STOPPED WORKING. MULTIPLE ATTEMPTS WERE MADE TO OBTAIN THE DEVICE FOR INVESTIGATION AND FURTHER INFORMATION FOR THIS COMPLAINT. NO RESPONSE WAS RECEIVED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10139542 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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