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Class I: serious health riskTerminated

Shakti Group 1) Compounded Asafoetida Powder L Recall

1) COMPOUNDED ASAFOETIDA POWDER L

SHAKTI GROUP USA LLC · New Brunswick, NJ

Risk level
Class I
Reported by FDA
Apr 27, 2016
Recall ID
F-1121-2016
Check your lot numberHow we source this data

Summary

Shakti Group recalled 1) Compounded Asafoetida Powder L starting Jan 7, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-1121-2016 on Apr 27, 2016. Reason: L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella. Status: Terminated.

Why it was recalled

L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.

Product description

1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED AT: LALJEE GODHOO & CO. Plot No. 53/4, Road 7/15, M.I.D.C.,Andheri (E). Mumbai - 400 093. (INDIA) Lot No., Pkd & Best Before See Bottom LOT NO. 2323" 2) COMPOUNDED ASAFOETIDA POWDER L.G¿, NET WT. 100g (3.5OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED AT: LALJEE GODHOO & CO. Plot No. 53/4, Road 7/15, M.I.D.C., Andheri (E). Mumbai - 400 093. (INDIA) Lot No., Pkd & Best Before See Bottom LOT NO. 2323"

Lot numbers, UPCs & expiration codes

Lot 2323

Where it was sold

NH, NJ, PA, OH & VA

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-1121-2016
Classification
Class I
Status
Terminated
Recall initiated
Jan 7, 2016
FDA report date
Apr 27, 2016
Quantity
approximately 10000 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
SHAKTI GROUP USA LLC

Original FDA data

Every field from FDA enforcement report F-1121-2016, exactly as published.

Show all FDA fields
City
New Brunswick
State
NJ
Status
Terminated
Country
United States
Event ID
73020
Address
14 van Dyke Ave
Code information
Lot 2323
Postal code
08901-3253
Report date
Apr 27, 2016
Product type
Food
Recall number
F-1121-2016
Classification
Class I
Recalling firm
SHAKTI GROUP USA LLC
Product quantity
approximately 10000 bottles
Termination date
Oct 23, 2017
Reason for recall
L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.
Voluntary / mandated
Voluntary: Firm initiated
Product description
1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED AT: LALJEE GODHOO & CO. Plot No. 53/4, Road 7/15, M.I.D.C.,Andheri (E). Mumbai - 400 093. (INDIA) Lot No., Pkd & Best Before See Bottom LOT NO. 2323" 2) COMPOUNDED ASAFOETIDA POWDER L.G¿, NET WT. 100g (3.5OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED AT: LALJEE GODHOO & CO. Plot No. 53/4, Road 7/15, M.I.D.C., Andheri (E). Mumbai - 400 093. (INDIA) Lot No., Pkd & Best Before See Bottom LOT NO. 2323"
Distribution pattern
NH, NJ, PA, OH & VA
Recall initiation date
Jan 7, 2016
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 20, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1121-2016, published Apr 27, 2016. View the source record (openFDA) · FDA enforcement reports

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

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