Pedia-lax recall: CGMP Deviations
PEDIA-LAX 66ML; NDC/UPC 301320202205; OTC; ENEMA
Why was Pedia-lax recalled?
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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 distributed 02/23/2021 through 03/10/2021.
- Product
- PEDIA-LAX 66ML; NDC/UPC 301320202205; OTC; ENEMA
- Recalling firm
- Cardinal Health Inc.
- Quantity
- 147
- Distribution
- FL, GA, SC
- Recall date
- June 2, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)