SRS Nutra LTD Physio Flex Joint Support Capsules Recalled for Undeclared Shellfish
NutraCap Labs LLC is recalling SRS Nutra LTD Physio Flex Joint Support Capsules due to undeclared shellfish in the product. Consumers with shellfish allergies should not use this product.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: This is an FDA Class I recall involving undeclared shellfish, a major allergen. Allergen mislabeling on common allergens without reported illness would typically be scored as 3 (High), but the FDA's Class I classification elevates this to 4 (Severe) per the rubric, which states that FDA Class I recalls never go below 4.
Plain-English summary
NutraCap Labs LLC is recalling SRS Nutra LTD Physio Flex Joint Support Capsules (60ct Bottle, Lot #2109360, Expiration Date 09/2023) because the product contains undeclared shellfish. This was discovered during an FDA investigation.
Approximately 80,169 bottles and jars were distributed across 25 states: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MN, NC, NJ, NV, NY, OH, OR, SC, TN, TX, VA, and WA.
Shellfish is a major allergen. Consumers who have a shellfish allergy and have purchased this product should not use it and should consult with a healthcare provider if they have consumed it and experience symptoms of an allergic reaction. Consumers should contact NutraCap Labs LLC or their retailer with questions.
The recalled product
- Product
- SRS Nutra LTD Physio Flex Joint Support Capsules 60ct Bottle NO UPC CODE
- Manufacturer
- NutraCap Labs LLC
- Category
- Food — Dietary Supplement
- Affected units
- 80,169
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)
- LOT # 2109360 EXP DATE 09/2023
Distribution
Part of a larger recall action
This product is one of 106 recalled by NutraCap Labs LLC 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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