Kwik-stik recall
KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.
Why was Kwik-stik recalled?
Potential that products packaged for lot 726-57-10 were packaged in pouches labeled as 323-108-7.
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?
Catalog Number: 0726P, Lot Number: 726-57-10, UDI: 20845357017486
- Product
- KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.
- Recalling firm
- Microbiologics Inc
- Quantity
- 65 packs (130 units)
- Distribution
- Worldwide distribution - US distribution in the states of GA, MS, MT, NC, NM, NV, TN, TX, WA, WI and the countries of Brazil, Canada, China, Colombia, Dominican Republic, France, India, Ireland, Japan, Mexico, Oman, Philippines, Romania, South Africa, Turkey, United Arab Emirates.
- Recall date
- February 9, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)