Wave Prep Tubes recall: Contamination
Wave Prep Tubes (1710-03) and single use cups (17--00-24)
Why was Wave Prep Tubes recalled?
Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug Administration inspection on October 15, 2019 were tested and found to be contaminated with Burkholderia cepacia. Mavidon is recalling all products manufactured at their facility.
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?
All Lots
- Product
- Wave Prep Tubes (1710-03) and single use cups (17--00-24)
- Recalling firm
- Carroll-Baccari, Inc.
- Quantity
- 1444 units
- Distribution
- Nationwide, Canada, UK, Spain, Australia
- Recall date
- April 1, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)