BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Reported: July 17, 2024 Initiated: June 12, 2024 #Z-2251-2024
Product Description
BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Reason for Recall
Sterilization certificates could not be validated by the supplier
Details
- Recalling Firm
- Synergetics Inc
- Units Affected
- 14 units
- Distribution
- US Nationwide
- Location
- O Fallon, MO
Frequently Asked Questions
What product was recalled? ▼
BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye). Recalled by Synergetics Inc. Units affected: 14 units.
Why was this product recalled? ▼
Sterilization certificates could not be validated by the supplier
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 17, 2024. Severity: Critical. Recall number: Z-2251-2024.
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