Bausch+lomb recall
BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Why was Bausch+lomb recalled?
Sterilization certificates could not be validated by the supplier
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?
UDI/DI 20841305107544, Lot Number P62764979R
- Product
- BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
- Recalling firm
- Synergetics Inc
- Quantity
- 14 units
- Distribution
- US Nationwide
- Recall date
- July 17, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)