Kimberly-Clark RadiOpaque Radiofrequency Cannula recall
Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Kimberly-Clark,Product code…
Why was Kimberly-Clark RadiOpaque Radiofrequency Cannula recalled?
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.
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?
Lot M3085K301 and M2327K301
- Product
- Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Kimberly-Clark,Product code…
- Recalling firm
- Kimberly-Clark Corporation
- Quantity
- 55 cases (10 units per case = 550 units)
- Distribution
- US Distribution in states of: AZ, CA, DE, FL, LA, MD, MA, NJ, NY, OH, PA and TX.
- Recall date
- February 5, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)