Halyard 43056Recalls & reported problems
Avanos Medical, Inc. · HYHSURGPN,ON-Q_QUIKBLO,N-STIM,-,20GX100, · Class 2
- 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 10680651430561), received between Dec 18, 2019 and Dec 18, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 18, 2019Break; Break
HOLD FOR MARCIA 4/2FILL VOLUME: UNKNOWN. FLOW RATE: UNKNOWN. PROCEDURE: A FASCIA ILIAC BLOCK FOR HIP FRACTURE. CATHPLACE: UNKNOWN. IT WAS REPORTED A QUIKBLOC NEEDLE HUB BROKE OFF FROM THE BASE OF THE NEEDLE. THERE WAS NO REPORTED PATIENT INJURY REPORTED. ADDITIONAL INFORMATION RECEIVED 26-NOV-2019 STATED A BOLUS WAS GIVEN THROUGH THE NEEDLE WITHOUT INCIDENT. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9489438 ↗
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- BD Luer-Lok, BD Glaspak 405672Becton, Dickinson And Company · Anesthesia conduction kit1 recall27 reports
- BD Luer-Lok, BD Glaspak 405673Becton, Dickinson And Company · Anesthesia conduction kit1 recall10 reports
- BD Luer-Lok, BD Glaspak 405637Becton, Dickinson And Company · Anesthesia conduction kit1 recall7 reports
- BD Luer-Lok, BD Glaspak 405707Becton, Dickinson And Company · Anesthesia conduction kit1 recall4 reports
- BD Luer-Lok, BD Glaspak 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405735Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.