Urgent Product Recall Notification (Initiated 04-07-2015)
Pharmedix® is requesting the return of the following product manufactured by Akorn as follows:
| Level of Recall: | RETAIL |
| Product Name: | Ful-Glo Strips |
| Manufacturer: | Akorn |
| NDC Code# | 17478-404-01 |
| PMX Order Code | PB00802 |
| Mnfct Lot #s | 8980, 9081, 9088, 9128, 9158 |
| PMX Lot#’s | 14223-001, 14233-001 |
| Reason for Recall | Recalled due to a packaging defect potentially impacting the amount of available fluorescein. |
This voluntary recall is extended to the RETAIL level and is being made with the knowledge of the Food and Drug Administration (FDA). This recall is only to your CLINIC LEVEL. You DO NOT need to contact any clients to whom the product was dispensed.
Our records show that product with the referenced Lot #(s) has/have been shipped to your clinic. Please examine your inventory to verify if you have product from these lots remaining in stock. If so, please discontinue dispensing it and quarantine the product.
Please complete the last column in the box below and fill in the # of units remaining in stock. If you do not have any recalled product left, put a zero. Then sign where indicated and fax this form back to Pharmedix® at 1-800-783-2038 even if you do not have any product from the indicated Lot #(s) remaining in stock. Once this completed form is sent back to Pharmedix® and you do have recalled product to return to Pharmedix®, you will receive pre-approved paperwork for returning the recalled product. Complete the paper as instructed and follow the directions for packing and shipping the recalled product. Pharmedix® will issue a UPS call tag to pick-up the recalled product and then issue you credit to your account.
If you have any additional questions, call Pharmedix® Customer Service at 1-800-486-1811, Ext. 14
Sincerely,
Richard J. Mangini, PharmD
Pharmedix® Client Services