Carfagna's Mild Chili Ready Sauce Recalled for Process Documentation Issue
Carfagna's Inc. is recalling 1,640 jars of Mild Chili Ready Sauce because the acidified process documentation was not on file with the FDA.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II but involves a documentation issue (process not on file) rather than a confirmed contamination or injury, fitting the 'Moderate' criteria for minor labeling/documentation errors or low-risk issues.
Plain-English summary
Carfagna's Inc. is voluntarily recalling 1,640 jars of Carfagna's Mild Chili Ready Sauce in 32 oz. glass jars. The recall is being conducted because the acidified process for the product was not on file with the U.S. Food and Drug Administration.
The affected product is identified by the manufacturing code 50340. The recall is limited to distribution in Ohio. The FDA has classified this recall as Class II, indicating that there is a reasonable probability that the use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences.
Consumers who have purchased this product should check their pantries for the specific manufacturing code and stop using the product if it matches the description. No specific instructions for disposal or return are provided in the source text.
The recalled product
- Product
- Carfagnas Mild Chili Ready Sauce in 32 oz. glass jars.
- Manufacturer
- Carfagnas Inc
- Category
- Food — Sauces
- Hazard
- Affected units
- 1,640
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)
- Manufacturing code: 50340
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 2 recalled by Carfagnas 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.
See all 2 products in this recall →Related recalls
Same manufacturer · Carfagnas Inc
See all →- ModerateCarfagnas Spicy Chili Ready Sauce Recalled for Missing Acidification Records
FDA (Food) · 2016-09-07
Same hazard · documentation issue
See all →- LowBMC Medical Luna G3 APAP Devices Recalled for Retroactive Rework Reporting
FDA (Devices) · 2026-08-26
- LowFARASTAR Cardiac Ablation Generator Recall for Missing Catheter Information
FDA (Devices) · 2026-07-29
- ModerateFARASTAR Ablation Generator EU Medical Device Recall for Labeling Discrepancy
FDA (Devices) · 2026-07-29
- LowPenner bathing spa 350010 series recalled for lacking unique device identifier
FDA (Devices) · 2026-03-18
- LowPenner bathing spa models recalled for lacking a unique device identifier
FDA (Devices) · 2026-03-18