16 Fr HemoStar XK Long-Term Hemodialysis Catheter recall
16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an AirGuard introducer. The device is used for patients requiring…
Why was 16 Fr HemoStar XK Long-Term Hemodialysis Catheter recalled?
Bard Access Systems is recalling one lot of 16 Fr HemoStar XK Long Term Hemodialysis Catheters because they were identified with an incorrect expiration date, 03/2015 rather than 10/2013.
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?
Product Code 5883730 lot number REVK0125.
- Product
- 16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an AirGuard introducer. The device is used for patients requiring…
- Recalling firm
- Bard Access Systems
- Quantity
- 120 units
- Distribution
- National US distribution only: MO, KS, AZ, OK, OR, AL, MA, TX, FL, MI, OH, LA, NJ, NC, WA, AR.
- Recall date
- September 5, 2012
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)