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Class II: temporary or reversible health riskTerminated

American Laboratories Xylanase 10 Recall

Xylanase 10,000XU/g, powder, enzyme, 100 gm

American Laboratories Inc · Omaha, NE

Risk level
Class II
Reported by FDA
Nov 13, 2013
Recall ID
F-0091-2014
Check your lot numberHow we source this data

Summary

American Laboratories recalled Xylanase 10 starting Sep 30, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0091-2014 on Nov 13, 2013. Reason: The products may be contaminated with Chloramphenicol. Status: Terminated.

Why it was recalled

The products may be contaminated with Chloramphenicol.

Product description

Xylanase 10,000XU/g, powder, enzyme, 100 gm. Product 45A

Lot numbers, UPCs & expiration codes

Lot ALI13206-05; re-evaluation date 1/25/2015 **sample only - not tested

Where it was sold

Distribution was made to IA, UT, NV, NE and CA.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0091-2014
Classification
Class II
Status
Terminated
Recall initiated
Sep 30, 2013
FDA report date
Nov 13, 2013
Quantity
1 sample bottle, 100 gm
Recall type
Voluntary: Firm initiated
Recalling firm
American Laboratories Inc

Original FDA data

Every field from FDA enforcement report F-0091-2014, exactly as published.

Show all FDA fields
City
Omaha
State
NE
Status
Terminated
Country
United States
Event ID
66445
Address
4410 S 102nd St
Code information
Lot ALI13206-05; re-evaluation date 1/25/2015 **sample only - not tested
Postal code
68127-1003
Report date
Nov 13, 2013
Product type
Food
Recall number
F-0091-2014
Classification
Class II
Recalling firm
American Laboratories Inc
Product quantity
1 sample bottle, 100 gm
Termination date
Apr 16, 2014
Reason for recall
The products may be contaminated with Chloramphenicol.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Xylanase 10,000XU/g, powder, enzyme, 100 gm. Product 45A
Distribution pattern
Distribution was made to IA, UT, NV, NE and CA.
Recall initiation date
Sep 30, 2013
Initial firm notification
Telephone
Center classification date
Nov 6, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0091-2014, published Nov 13, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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