# TIANJIN HUBAO CONDIMENTS BREWING CO.,LTD. · 99-37 · CHINA — FDA import alert red lists: firms subject to detention without physical examination

For TIANJIN HUBAO CONDIMENTS BREWING CO.,LTD. · 99-37 · CHINA, import alert is 99-37; import alert name is "DETENTION WITHOUT PHYSICAL EXAMINATION OF LOW-ACID CANNED FOODS AND ACIDIFIED FOODS WITHOUT FILED SCHEDULED PROCESSES"; country is CHINA; product is Soybean Paste Products | Soybean Paste Products | Soybean Paste Products | Soybean Paste Products; product code is 23 R - - 03 Soybeans (Edible Seed Paste) | 24 A - - 13 Soybeans (See Industry 37 for 'Bean Curd') | 24 B - - 13 Soybeans (See Industry 37 for Bean Curd), Dried or Paste | 37 K - - 15 Bean, Yellow Paste; date published is 07/10/2026; address is Economic Development Zone , No. 12 Bayi Road; Jingji Development Zone , Ji County, Tianjin CHINA, verified against its source on 2026-09-16.

- **Firm:** TIANJIN HUBAO CONDIMENTS BREWING CO.,LTD. _(verified: appears in the quote below)_
- **Import alert:** 99-37
- **Import alert name:** "DETENTION WITHOUT PHYSICAL EXAMINATION OF LOW-ACID CANNED FOODS AND ACIDIFIED FOODS WITHOUT FILED SCHEDULED PROCESSES"
- **Country:** CHINA _(verified: appears in the quote below)_
- **Address:** Economic Development Zone , No. 12 Bayi Road; Jingji Development Zone , Ji County, Tianjin CHINA _(verified: appears in the quote below)_
- **Date published:** 07/10/2026 _(verified: appears in the quote below)_
- **Product code:** 23 R - - 03 Soybeans (Edible Seed Paste) | 24 A - - 13 Soybeans (See Industry 37 for 'Bean Curd') | 24 B - - 13 Soybeans (See Industry 37 for Bean Curd), Dried or Paste | 37 K - - 15 Bean, Yellow Paste _(verified: each item appears in the quote below)_
- **Product:** Soybean Paste Products | Soybean Paste Products | Soybean Paste Products | Soybean Paste Products _(verified: each item appears in the quote below)_
- **FDA notes:** FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container. | FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container. | FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container. | FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container. _(verified: each item appears in the quote below)_

## What the source says

> TIANJIN HUBAO CONDIMENTS BREWING CO.,LTD. Date Published : 07/10/2026 Economic Development Zone , No. 12 Bayi Road; Jingji Development Zone , Ji County, Tianjin CHINA 23 R - - 03 Soybeans (Edible Seed Paste) Date Published: 07/10/2026 Desc: Soybean Paste Products Notes: FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container. 24 A - - 13 Soybeans (See Industry 37 for 'Bean Curd') Date Published: 07/10/2026 Desc: Soybean Paste Products Notes: FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container. 24 B - - 13 Soybeans (See Industry 37 for Bean Curd), Dried or Paste Date Published: 07/10/2026 Desc: Soybean Paste Products Notes: FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container. 37 K - - 15 Bean, Yellow Paste Date Published: 07/10/2026 Desc: Soybean Paste Products Notes: FDA inspection found serious deviations of LACF regulation (21 CFR 113) and Emergency Permit Control regulation (21CFR 108). The firm’s LACF food products appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act (the Act). Specifically:• 21 CFR 108.25(c)(2)- Information on the scheduled process for a new low-acid canned food prior to packing the food was not provided. • 21 CFR 113.100(b)- An entry on a production record was not made at the time the specific retort or processing system condition or operation occurred. • 21CFR 113.60(a)(3)- Appropriate detailed inspections and tests of containers were not conducted at intervals of sufficient frequency to ensure proper closing machine performance and consistently reliable hermetic seal production. • 21 CFR 108.35(g)- Operators of processing systems and product formulating systems are not under the operating supervision of a person that has attended and satisfactorily completed, a school approved by the Commissioner. • 21 CFR 113.60(c)- The identification code for hermetically sealed containers did not identify in code the establishment where packed or product in the container.

## Source

- https://www.accessdata.fda.gov/cms_ia/importalert_1131.html

Last verified: 2026-09-16. Review by: 2026-11-15.
Part of [FDA import alert red lists: firms subject to detention without physical examination](https://referencesource.org/fda-import-alert-red-list/).