EB 110311-01, powder, enzyme blend, packaged in 5 kg double poly bags inside fiber box. Product 73C
Recalling firm: American Laboratories Inc
Why it was recalled
The products may be contaminated with Chloramphenicol.
The exact product
EB 110311-01, powder, enzyme blend, packaged in 5 kg double poly bags inside fiber box. Product 73C
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot # ALI13200-09, re-evaluation date 1/19/2015; Lot # ALI13140-03, re-evaluation date 11/20/2014; Lot # ALI13071-01, re-evaluation date 9/12/2014 and Lot # ALI13008-01; re-evaluation date 7/8/2014. **Lot ALI13200-09 mathmatical analysis tested "probably < 0.3 ppb in final product" **the other three lots mathmatical analysis tested "probably NOT < 0.3 ppb in final product"
| Type | Code / value | Context |
|---|---|---|
| lot | ALI13008-01 | tion date 11/20/2014; Lot # ALI13071-01, re-evaluation date 9/12/2014 and Lot # ALI13008-01; re-evaluation date 7/8/2014. **Lot ALI13200-09 mathmatical analysis tested "probably < 0.3 ppb in final product" |
| lot | ALI13071-01 | luation date 1/19/2015; Lot # ALI13140-03, re-evaluation date 11/20/2014; Lot # ALI13071-01, re-evaluation date 9/12/2014 and Lot # ALI13008-01; re-evaluation date 7/8/2014. **Lot ALI13200-09 mathmatical anal |
| lot | ALI13140-03 | Lot # ALI13200-09, re-evaluation date 1/19/2015; Lot # ALI13140-03, re-evaluation date 11/20/2014; Lot # ALI13071-01, re-evaluation date 9/12/2014 and Lot # ALI13008-01; re-evaluation da |
| lot | ALI13200-09 | Lot # ALI13200-09, re-evaluation date 1/19/2015; Lot # ALI13140-03, re-evaluation date 11/20/2014; Lot # ALI13071-01, re-evaluation date |
Recall details
- Recall number
- F-0096-2014
- Event ID
- 66445
- FDA status
- Terminated
- Initiated
- Sep 30, 2013
- Reported
- Nov 13, 2013
- Classified
- Nov 6, 2013
- Terminated
- Apr 16, 2014
- Quantity
- 4/5 KG-boxes
- Location
- Omaha, NE, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
Distribution was made to IA, UT, NV, NE and CA.
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.