Xylanase 150,000XU, powder, enzyme, 100 gm. Product 13A
Recalled by American Laboratories INC on Sep 30, 2013
Recall Summary
American Laboratories INC recalled Xylanase 150,000XU, powder, enzyme, 100 gm. Product 13A in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Sep 30, 2013.
The FDA-published reason for this recall is: "The products may be contaminated with Chloramphenicol."
The product reached multiple states, recorded by the FDA as "Distribution was made to IA, UT, NV, NE and CA." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Omaha, NE. The recall covers 1 sample bottle, 100 gm of product. The FDA has Terminated this recall (first reported Nov 13, 2013), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.
Reason for Recall
The products may be contaminated with Chloramphenicol.
Product Description
Xylanase 150,000XU, powder, enzyme, 100 gm. Product 13A
Distribution
Distribution was made to IA, UT, NV, NE and CA.
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Browse Related Recalls
Terms Explained
- Class II Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.