T & R Enterprises Recalls Crab Rangoon Due to Insanitary Conditions
T & R Enterprises USA, Inc. is recalling 1.0 oz. Crab Rangoon produced under insanitary conditions. The product was distributed to food service distributors in California and Michigan.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II. According to the rubric, an FDA Class II recall is assigned a severity score of 4 (Severe), particularly when associated with significant risk factors like insanitary conditions.
Plain-English summary
T & R Enterprises USA, Inc. is voluntarily recalling 1.0 oz. Crab Rangoon. The recall is due to the product being produced and packaged under insanitary conditions. The affected product is identified by code dates ranging from 080119 to 092619.
The recalled product was distributed to food service distributors in California and Michigan. The product quantity is listed as 600/100/1 oz/eggrolls/cases.
Consumers who have purchased this product should check their inventory for the specific code dates and stop using the product. They should contact the recalling firm for further instructions or a refund.
The recalled product
- Product
- Crab Rangoon 1.0 oz.
- Manufacturer
- T & R Enterprises USA, Inc.
- Category
- Food — Frozen Prepared Foods
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 080119 to 092619
Distribution
Part of a larger recall action
This product is one of 2 recalled by T & R Enterprises USA, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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