ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC recall
ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) central…
Why was ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC recalled?
Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
CDA-42802-P1A CDA-42854-P1A CDA-45703-P1A 13F16K0239 13F16L0285 13F17C0318 13F16L0071 13F16M0048 13F17E0124 13F17F0497 13F17G0428 13F17H0387 13F16K0306 13F16L0091 13F17A0167 13F17B0145 13F17C0174 13F17C0466 13F17E0095 13F17F0261 13F17G0090 13F17G0541 13F17H0566 CDA-47702-P1A 13F17B0249
- Product
- ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) central…
- Recalling firm
- Arrow International Inc
- Quantity
- 23,904 in total
- Distribution
- US in the states of OH, FL, SC, TX, KY, NJ, MI
- Recall date
- March 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)