Tense-X supplement recalled because it contains magnesium salicylate
Professional Botanicals is recalling 253 bottles of Tense-X capsules because the product contains magnesium salicylate.
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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Scored 3 under the risk-of-harm criterion: an undisclosed pharmacologically active salicylate in a supplement can reach people who must avoid it, and no illnesses are reported.
Plain-English summary
Tense-X, in 175cc HDPE bottles of 60 vegetable capsules with a two-capsule dose, product SKU PB207, from Professional Botanicals, is being recalled because the product contains magnesium salicylate.
The recall covers 253 bottles from lot 290301. The product was distributed nationwide, including Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota and Missouri. The FDA has classified the recall as Class II.
Salicylates are avoided by people with a salicylate sensitivity and by others on medical advice, so an undisclosed salicylate in a supplement matters. The enforcement record reports no illnesses.
Anyone holding a bottle from lot 290301 should stop taking it and contact the firm or their prescriber.
The recalled product
- Product
- Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207
- Manufacturer
- Professional Botanicals, Inc.
- Category
- Food — Dietary supplement
- Affected units
- 253
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 #: 290301
Distribution
Part of a larger recall action
This product is one of 3 recalled by Professional Botanicals, 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 3 products in this recall →Related recalls
Same manufacturer · Professional Botanicals, Inc.
See all →- HighNutra Calm supplement recalled because it contains magnesium salicylate
FDA (Food) · 2025-11-19
- HighDietary supplement recalled because it contains magnesium salicylate
FDA (Food) · 2025-11-19
Same hazard · undeclared ingredient
See all →- HighEl Ruisenor De Mexico Recalls Fritura Lagrimita Wheat Snack for Allergens
FDA (Food) · 2026-10-28
- HighEl Ruisenor Tropical Trail Mix Recalled for Undeclared Allergens
FDA (Food) · 2026-10-28
- HighJovy Gummy Worms Recalled for Undeclared Artificial Dye Ingredients
FDA (Food) · 2026-10-28
- ModerateWise Onion Rings recalled for undeclared food color additives
FDA (Food) · 2026-07-15
- ModerateDietary Supplement Vista MAX Recalled for Undeclared Yellow #5 Allergen
FDA (Food) · 2026-07-08
Similar recalls
- CriticalNaturect Capsules Recalled for Undeclared Tadalafil Ingredient
FDA (Drugs) · 2014-05-28
- ModerateAstraZeneca Recalls Nexium Capsules Due to Foreign Product Contamination
FDA (Drugs) · 2012-07-18
- CriticalTiger-X Dietary Supplement Recalled for Undeclared Sildenafil
FDA (Drugs) · 2016-10-26
- SevereMALEXTRA Dietary Supplement Recalled for Undeclared Pharmaceutical Ingredients
FDA (Drugs) · 2025-06-18
- CriticalGinseng Power-X Recalled for Undeclared Sildenafil
FDA (Drugs) · 2016-10-26
- SevereP-Boost Capsules Recalled for Undeclared Tadalafil Ingredient
FDA (Drugs) · 2014-05-28