Medline medical procedure kits labeled as follows: a) recall
Medline medical procedure kits labeled as follows: a) C-SECTION CDS, REF CDS983998C
Why was Medline medical procedure kits labeled as follows: a) recalled?
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
a) REF CDS983998C, UDI/DI 40193489776714 (case), 10193489776713 (unit), Lot Numbers: 22HBC905, 22HBZ254, 23ABI006, 23CBJ920, 23EBN740, 23FBT058, 23GBR762, 23GBR790, 23JBN978, 23KBT038
- Product
- Medline medical procedure kits labeled as follows: a) C-SECTION CDS, REF CDS983998C
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1753 units
- Distribution
- Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
- Recall date
- August 28, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)