Hypromellose Recall: Aurolab Trust FOCUS PI
FDA recalls Aurolab Trust FOCUS PI Hypromellose 0.7% Formula, 0.3 FL OZ per vial, sterile, manufactured for Covalent Management, Inc. The recall covers Batch# 6B093FI (Exp. 04/01/28) and Batch# 6F511F1 (Exp. 05/15/28), with about 25,220 bottles distributed in Virginia. No corrective action is listed in the recall notice.
| Brand | Aurolab Trust |
|---|---|
| Product | FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent Management, Inc., Manassas, VA 20109. NDC: 82724-007-19 |
| Reason | Lack of Assurance of Sterility |
| Severity | moderate |
| Units affected | 25220 |
| Distribution | VA |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use any vials from batches 6B093FI or 6F511F1.
- Set aside any affected product and contact Covalent Management, Inc. for disposal/return instructions or talk to your healthcare provider for alternatives.
- If you have used the product and have concerns, seek medical advice.
- Refer to the FDA recall notice for updates and additional instructions.
How to identify the recalled item
| Lot / date codes | Batch# 6B093FI, Exp. 04/01/28; Batch# 6F511F1, Exp. 05/15/28 |
|---|---|
| Lot / date codes | Batch# 6B093FI, Exp. 04/01/28; Batch# 6F511F1, Exp. 05/15/28 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.