Titan Potato Puffs Recalled for Undeclared Sodium Bisulfite Ingredient
Empresas Barsan, Inc. is recalling Titan Potato Puffs with Meat Flavor because the label fails to declare Sodium Bisulfite as an ingredient.
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 and involves a labeling error regarding an undeclared ingredient (Sodium Bisulfite), which fits the rubric for minor labeling errors or low-risk contamination.
Plain-English summary
Empresas Barsan, Inc. is voluntarily recalling 1,440 units of TITAN, 6 rellenos, Potato Puffs with Meat Flavor, Net Weight 26.4 oz (748g). The recall is being conducted because the finished product label does not declare Sodium Bisulfite as an ingredient.
The affected product is identified by yellow stick-on labels marked "Expira 12/12/18" (Expire 12/12/18) and "Expira 12/14/18" (Expire 12/14/18). The recall is limited to Puerto Rico.
Consumers who have purchased this product should check their labels for the specific expiration dates and contact the recalling firm for further instructions.
The recalled product
- Product
- TITAN, 6 rellenos, Potato Puffs with Meat Flavor, Net Weight 26.4 oz (748g)
- Manufacturer
- Empresas Barsan, Inc.
- Category
- Food — Snacks
- Hazard
- Affected units
- 1,440
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 2 recalled by Empresas Barsan, 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 · Empresas Barsan, Inc.
See all →- ModerateTitan Potato Puffs Recalled for Undeclared Sodium Bisulfite Ingredient
FDA (Food) · 2018-02-14
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02