BD Microtainer Quikheel Lancet 1.0 mm incision Depth recall
BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lakes, NJ 07417…
Why was BD Microtainer Quikheel Lancet 1.0 mm incision Depth recalled?
The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
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?
REF # 368101 Lot #3116007 Class I Exempt Device listing Number E158602
- Product
- BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lakes, NJ 07417…
- Recalling firm
- Becton Dickinson & Company
- Quantity
- US - 39,800 units ; Canada - 18,400 units
- Distribution
- Distributed in the states of CT, KY, IL, NY, PA, TX, and VA and the country of Canada.
- Recall date
- September 18, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)