PerkinElmer 226 Sample Collection Device recall
PerkinElmer 226 Sample Collection Device
Why was PerkinElmer 226 Sample Collection Device recalled?
PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.
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?
UDI: (01)50812589020011(17)200831(10)40020001; Serial Numbers: 06879601-06879700
- Product
- PerkinElmer 226 Sample Collection Device
- Recalling firm
- PerkinElmer Health Sciences, Inc.
- Quantity
- 164,952 devices
- Distribution
- US distribution in the state of Ohio
- Recall date
- June 10, 2020
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)