CLASS II Device recall · Reported 26 Jun 2019 · FDA Enforcement Report
Arrowg+ard Blue Advance PICC Product recalled by Arrow International
Arrow International is recalling Arrowg+ard Blue Advance PICC, distributed nationwide in the US. The recall was initiated on 23 Apr 2019 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1811-2019
- FDA event ID
- 82865
- Recalling firm
- Arrow International, Reading, PA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 23 Apr 2019
- FDA classified
- 15 Jun 2019
- Reported
- 26 Jun 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 23 Apr 2019 | Recall initiated by company | |
| 15 Jun 2019 | Classified by FDA | +53 days |
| 26 Jun 2019 | Published in enforcement report | +11 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lidstock states the incorrect expiration date for the product
Product as listed by the FDA
Arrowg+ard Blue Advance PICC Product Code: CDC45541HPK1A
Where it was distributed
Nationwide Foreign:
Questions about this recall
Why was it recalled?
Lidstock states the incorrect expiration date for the product
Which lots are affected?
Batch Code: 23F17K0359, 23F18C0027, 23R17K0359
Where was it sold?
Nationwide Foreign:
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
35 other products · FDA event 82865This product is part of a recall event; the main page for the event is Arrow JACC with Chlorag+ard Technology Jugular Axillo recalled.
More recalls from Arrow International
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|---|---|---|---|---|---|
| Device | CLASS I | Description/REF: Agba Picc G4 Stylet: 3L 6FR x 55CM recalled | Arrow International | Sterility | Nationwide |
| Device | CLASS I | Description/REF: Hemodialysis KIT: 2-Lumen 8 FR X 11 CM/AK recalled | Arrow International | Sterility | Nationwide |
| Device | CLASS I | Description/REF: PI CVC KIT recalled by Arrow International | Arrow International | Sterility | Nationwide |
| Device | CLASS I | Description/REF: PI Picc: 3: 6FR x 55CM w CHG/ Dlx-35563-Hpkc; Agba recalled | Arrow International | Sterility | Nationwide |
| Device | CLASS I | Description/REF: Pacing PSI KIT: 6 FR/AI-06210-KS, Pacing PSI KIT recalled | Arrow International | Sterility | Nationwide |
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