Reported Sep 9, 2015 · Terminated

Arrow International, Inc. PICC Kits and VPS Access Kits with Touhy Borst Component Catheter, Intravascular,…

Arrow International Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Arrow International Inc · 2400 Bernville Rd · Reading, PA · 19605-9607

Is this the product you have?

  • Arrow International, Inc. PICC Kits and VPS Access Kits with Touhy Borst Component Catheter, Intravascular, Therapeutic, Ultrasound, Long Term Greater than 30 Days
Lot codes and dates
  • Material Nos.:
    • ASK-04001-DU4
    • ASK-04001-DU5
    • ASK-04001-DU6
    • ASK-04001-DU6
    • ASK-04001-DU7
    • ASK-04001-DU8
    • ASK-35052-JHVA1
    • ASK-45041-JHVA
    • CDC-44041-VPS
    • CDC-35063-VPS
    • CDC-35541-VPS
    • CDC-35552-VPS
    • CDC-35563-VPS
    • CDC-44041-VPS
    • CDC-45541-VPS
    • VPS7220B
    • CDC-34041-VPS
    • CDC-34052-VPS
    • CDC-34063-VPS
    • CDC-35041-VPS
    • CDC-35041-VPS
    • CDC-35052-VPS
    • CDC-35063-VPS
    • ASK-04001-DU5
    • CDC-45041-VPS
    • ASK-04001-UOC
    • ASK-35041-JHVA
    • ASK-35052-JHVA
    • CDC-34041-VPS
    • VPS7220B
    • VPS7220B
    • VPS7220B
    • VPS7220B
    Batch Nos.:

    251 of 251 codes

    • 23F14A1779
    • 23F14D0281
    • 23F14M0072
    • 23F14D1271
    • 23F14G0101
    • 23F14G1295
    • 23F14E1325
    • 23F15A1407
    • 23F14F0406
    • 23F15B1012
    • 23F14J0973
    • 23F14G0091
    • 23F15B1630
    • 23F14F0782
    • RF3053214
    • 23F14M0791
    • 23F14K1260
    • RF3052236
    • 23F14J1421
    • 23F13M0751
    • 23F13L0144
    • 23F14L0635
    • RF3052644
    • 23F14K1255
    • 23F14D0332
    • 23F14B1160
    • 23F15B1628
    • RF3064510
    • 23F14M0026
    • 23F14G0107
    • 23F14D0759
    • RF3042008
    • 23F14A0375
    • 23F14A1189
    • 23F14J1433
    • 23F14F1092
    • 23F13M0589
    • 23F14A1493
    • 23F14B1128
    • 23F15A0122
    • 23F14G0916
    • 23F14A0451
    • 23F14B0740
    • 23F14C0473
    • RF3053218
    • 23F14H0046
    • 23F14A1495
    • 23F14B1120
    • 23F14D0308
    • 23F14A1277
    • 23F14J1319
    • 23F14B0056
    • 23F14C0463
    • 23F14J1391
    • 23F14D0378
    • 23F14K1292
    • 23F14B0742
    • 23F14D0286
    • 23F14K1472
    • 23F14F0284
Amount recalled
92902

Where it was sold

  • Nationwide

Why it was recalled

saline leakage from unsecured connections between the Touhy Borst adaptor and the hub of the catheter. No injuries reported.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 26, 2018 · Data as of Sep 19, 6:05 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.