RecallHawk
Class II Recall

Vandevi Compounded Asafoetida 50 gm, 100 gms 200 gm, 500 gm, 1 kg. Packaged in yellow plastic bottles with plastic shrin

KINJIN FOOD PRIVATE LIMITED

Summary

The FDA issued a Class II for Vandevi Compounded Asafoetida 50 gm, 100 gms 200 gm, 500 gm, 1 kg. Packaged in y by KINJIN FOOD PRIVATE LIMITED. Reason: Undeclared wheat.

Details

Source

Food Recall

External ID

F-0908-2024

Action Date

2024-02-28

Status

Terminated

Category

food

Product Description

Vandevi Compounded Asafoetida 50 gm, 100 gms 200 gm, 500 gm, 1 kg. Packaged in yellow plastic bottles with plastic shrink wrap blue/yellow labels.

Lot/Code Info: Batch 163 Expiration/Best Before Dates: NOV- 2023, 06-NOV-2023, 08-DEC-2023, 23-DEC-2023, 05-DEC-2023, 10-NOV-2023, 14-DEC-2023, 13-02-2024, & 10-NOV-2023 Batch 169 Expiration/Best Before Dates: DEC- 2023, 24-FEB-2024, 03-APR-2024, 08-MAY-2024, 05-JUN-2024, 03-JUL-2024, 09-JUN-2024, 25-MAR-2024, 04-MAR-2024, 06-MAY-2024, 08-MAR-2024, 08-MAY-2024, 22-FEB-2024, MAY-2024 &03-JUN-2024 Batch 173 Expiration/Best Before Dates: 11-NOV-2024, 20-NOV-2024, 11-NOV-2024, 11-JUL-2024, 01-AUG-2024, 08-AUG-2024, 14-SEP-2024, 11-NOV-2024, 12-DEC-2024, 13-JUL-2024, 19-AUG-2024 & 25-SEP-2024 Batch 178 Expiration/Best Before Dates: DEC- 2024, FEB- 2025, 19-MAR-2025, 09-MAR-2025, 18-JAN-2025, 09-APR-2025, 07-MAY-2025, 13-FEB-2025, 02-APR-2025, 10-MAY-2025 01-03-2025 & 02-MAY-2025 Batch 181 Expiration/Best Before Dates: SEP- 2025, 08-JUN-2025, 13-JUL-2025, 14-SEP-2025, 24-JUL-2025, 22-AUG-2025, 14-JUN-2025, 05-JUN-2025, 07-JUL-2025, 06-AUG-2025 10-SEP-2025, 10-SEP-2025, 15-AUG-2025, 01-SEP-2025 &22-AUG-2025

Quantity Affected: 18,580 kg

Reason for Recall

Undeclared wheat

Distribution

Distributed to exporters in India who then distribute product to the US.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-02

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KINJIN FOOD PRIVATE LIMITED) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does KINJIN FOOD PRIVATE LIMITED have FDA actions?

This is the only FDA action we have on record for KINJIN FOOD PRIVATE LIMITED in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0908-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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