Kwik-stik recall
KWIK-STIK, Enterobacter cloacae subsp. cloacae derived from ATCC 13047, REF 0323P. Packaged 2 units per pack. IVD controls.
Why was Kwik-stik recalled?
Potential of products packaged for lot 323-108-7 were packaged in pouches labeled as 726-57-10.
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: 0323P, Lot Number: 323-108-7, UDI: 20845357006381
- Product
- KWIK-STIK, Enterobacter cloacae subsp. cloacae derived from ATCC 13047, REF 0323P. Packaged 2 units per pack. IVD controls.
- Recalling firm
- Microbiologics Inc
- Quantity
- 47 packs (94 units)
- Distribution
- US distribution to CA, FL, HI, MI, NC, NH, NJ, OK, OR, TN. International distribution to Canada, Ecuador, France, India, Indonesia, Ireland, Japan, Mexico, South Africa, United Arab Emirates, Vietnam.
- Recall date
- February 9, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)