Reported Sep 2, 2015 · Terminated

PICC Kits with Peel-Away Sheath Component; catheter, intravascular, therapeutic, ultrasound Product Usage: catheter,…

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?

  • PICC Kits with Peel-Away Sheath Component; catheter, intravascular, therapeutic
  • ultrasound Product Usagecatheter, intravascular, therapeutic, ultrasound
Lot codes and dates
  • Product Codes
    • ASK-02041-SEH1
    • CA-05052-HP
    • CDC-34052-VPS
    • EU-05552-HPMSB
    • ASK-04001-DU4
    • CA-05052-HPX
    • CDC-35041-VPS
    • FR-04041
    • ASK-04052-AC
    • CDC-02041-MK1A
    • CDC-35052-VPS
    • FR-04041-CF
    • ASK-05041-LM4
    • CDC-04041-HPK1A
    • CDC-35541-VPS
    • FR-05041
    • ASK-05052-SFL
    • CDC-04052-HPK1A
    • CDC-35552-VPS
    • FR-05041-CF
    • ASK-05541-MS2
    • CDC-05041-HPK1A
    • EU-04041-HP
    • FR-05541-CF
    • ASK-05541-MS3
    • CDC-05052-HPK1A
    • EU-04041-HPMSB
    • PI-01451-LS
    • ASK-15552-LM2
    • CDC-05541-HPK1A
    • EU-04052-HPMSB
    • PI-01451-LS5
    • ASK-15552-MS3
    • CDC-05542-PK1A
    • EU-05041-HPMSB
    • PK-01451-WS
    • ASK-35041-JHVA
    • CDC-05552-HPK1A
    • EU-05052-HPMSB
    • PK-01451-WSSP
    • CA-05041-HP
    • CDC-15552-HPK1A
    • EU-05541-HP
    • UK-05041-HPMIN
    • CA-05041-HPX
    • CDC-34041-VPS
  • EU-05541-HPMSB lot numbers

    209 of 209 codes

    • 23F14H0517
    • 23F14J0077
    • 23F15F0662
    • 71F14M0678
    • 71F15A1660
    • 23F14L0941
    • 23F15C2282
    • 23F14H0328
    • 71F15A0395
    • 71F15B1938
    • 23F14B1232
    • 23F14D0456
    • 23F14C0598
    • 71F15C0214
    • 71F15D0235
    • 23F15A1523
    • 23F14C0059
    • 23F14F1505
    • 71F15D0053
    • 71F14L1345
    • 23F14A1779
    • 23F14E1213
    • 23F14K1025
    • 71F15D1075
    • 71F15D1077
    • 23F14G1295
    • 23F14G1470
    • 23F15B0400
    • 23F14C0576
    • 71F15E0455
    • 23F14J0973
    • 23F14H1111
    • 23F14F1507
    • 23F14F0115
    • 71F14K1571
    • 23F14M0791
    • 23F14J0613
    • 23F14M0440
    • 23F14G1130
    • 71F14F1786
    • 23F15A1171
    • 23F15A0149
    • 23F14F0364
    • 23F14F0504
    • 71F14G1690
    • 23F14H0848
    • 23F15D0507
    • 23F14L0838
    • 23F14D0713
    • 71F14F1844
    • 23F14F0370
    • 23F14J1512
    • 23F14H0331
    • 23F14C0575
    • 71F14E2043
    • 23F15C2435
    • 23F15C0302
    • 23F15B0401
    • 23F14D0724
    • 71F14K0639
Amount recalled
52109

Where it was sold

  • Nationwide

Why it was recalled

the catheter peel-away component hub tabs may prematurely detach. One injury reported.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 28, 2018 · Data as of Sep 19, 4:52 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.