Hang&Go recall
Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120
Why was Hang&Go recalled?
The sterilization contractor informed the company of a quality issue possibly affecting the sterilization process of a certain number of products. It was determined that some lots may not be sterile.
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 Numbers: F180266 F180315 F190169
- Product
- Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120
- Recalling firm
- RanD S.r.l.
- Quantity
- 72
- Distribution
- The products were distributed to the following US states: FL, IL, TN, WI
- Recall date
- July 21, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)