ULTRA Fabric Reinforced Surgical Gown recall
ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use…
Why was ULTRA Fabric Reinforced Surgical Gown recalled?
The impacted product was not intended for commercial distribution to end users.
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?
Product Code: 95221-35, Unit Code: 90372
- Product
- ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use…
- Recalling firm
- Kimberly-Clark Corporation
- Quantity
- 32 cases
- Distribution
- US (nationwide) including the states of CA, CO, LA, NM, OK, TX and WA.
- Recall date
- September 26, 2012
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)