FDAClass IINovember 6, 2019

BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25 recall

BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608

Why was BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25 recalled?

BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.

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?

Lot 8207894 ***UPDATED 7/11/19*** Lots 9025826 and 8354527 ***UPDATED 12/10/19*** Lot 9010765

Product
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Recalling firm
Becton Dickinson & Company
Quantity
2,624,160 (2,169,703 US; 454,457 OUS)
Distribution
Distributed to accounts in AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, and VA. Foreign distribution to Canada, Brazil, India, Mexico, Singapore, and Taiwan.
Recall date
November 6, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls