ARROW IPN046022Recalls & reported problems
Teleflex Incorporated · FlexBlock(R) Continuous Peripheral Nerve Block Kit · Class 2
All models of ARROW (1494)
Data updated Oct 16, 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 50801902078525), received between May 5, 2026 and May 5, 2026 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Skin Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 5, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT "TWO PATIENTS WHO HAD PROCEDURES USING THE SAME KIT, DEVELOPED A DEEP INFECTION. BOTH PATIENTS NEEDED TO BE HOSPITALIZED AND HAD TO HAVE AN INCISION AND DRAINAGE OF AN ABSCESS WHICH FORMED ALONG THE CATHETER TRACT. THE NERVE BLOCK KIT USED ON BOTH PATIENTS HAD THE SAME LOT NUMBER". ADDITIONAL INFORMATION RECEIVED STATES THAT "[PATIENT] DEVELOPED SEVERE R. ARM PAIN AND IMMOBILITY, A R. NECK DEEP ABSCESS WITH MULTIPLE LOCULATIONS, REQUIRING I & D TWICE. THE FIRST I & D WAS AT BESIDE ON (B)(6) 2026, DRAIN LEFT IN PLACE. THE SECOND I & D WAS IN THE OR (B)(6) 2026 FOR FURTHER WASHOUT - TWO DRAINS LEFT (1 RED RUBBER, 1 PENROSE) IN THE DEPTH OF THE ABSCESS POCKET THAT WERE USED FOR IRRIGATION AND DRAINAGE. THE PATIENT WAS HOSPITALIZED FROM (B)(6) 2026 UNTIL (B)(6) 2026 AND WAS DISCHARGED HOME WITH HOME HEALTH ON (B)(6) 2026 WITH THE TWO DRAINS FOR IRRIGATION AND DRAINAGE. THE PENROSE AND RED RUBBER WERE REMOVED ON (B)(6) 2026 AND THE WOUND WAS PACKED BY THE HOME HEALTH RN. THE RIGHT IS IMMOBILE; PATIENT IS NOT ABLE TO LIFT IT BUT IS MOVING HIS FINGERS. SURGERY WAS ON (B)(6) 2026. CATHETER WAS REMOVED ON (B)(6) 2026, SYMPTOMS STARTED ON (B)(6) 2026 (NEW PAIN, NUMBNESS,
Patient problems: Skin Infection
MAUDE report 25086633 ↗
Other Anesthesia conduction kit devices
- BD Luer-Lok, BD Glaspak 405671Becton, Dickinson And Company · Anesthesia conduction kit1 recall68 reports
- ARROW IPN922678Teleflex Incorporated · Anesthesia conduction kit2 recalls0 reports
- 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 405735Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 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 · 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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