76%

Fewer recalls than
Supplements & Specialty peers

Beta Labs — FDA Recall History & Enforcement Records

Established Player · Supplements & Specialty

Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.

As of July 16, 2026, Beta Labs has 4 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 20 Jun 2013. Beta Labs is categorized under Supplements & Specialty based on their predominant recall history.

4
Total FDA recalls
13.1
Years in FDA database
0.3
Recalls per year
4,774 days(13.1 yrs)
Since last recall
25.0%
Class I (life-threatening)
0.3 recalls/yr vs Supplements & Specialty avg 2.3/yrWell Below Average

Recall activity over time for Beta Labs

How serious are Beta Labs recalls?

FDA recall classifications by severity

Class I (Life-threatening)
25.0% (1 recalls)
Class II (Moderate risk)
75.0% (3 recalls)
Class III (Minor violation)
0.0% (0 recalls)

Full FDA recall history for Beta Labs

All 4 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first

Date Product Reason Class & Status
20 Jun 2013Official FDA Notice PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements. Class ITerminated
20 Jun 2013Official FDA Notice PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements. Class IITerminated
20 Jun 2013Official FDA Notice RED VIPERS, ADVANCED FOCUS AND CONCENTRATION, HEIGHTENED ENERGY LEVELS, 75mg EPHEDRA, Manufactured for: Beta Labs, LTD The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements. Class IITerminated
20 Jun 2013Official FDA Notice Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSULES, Distributed by Beta Labs, LT The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements. Class IITerminated

Where have Beta Labs recalls occurred?

States affected across all recorded FDA enforcement actions

Nationwide

Where does this recall data come from?

Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.

Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.

To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.

© 2026 FoodRecallFinder.com | Turnkey Trading Unlimited LLC. All rights reserved. FDA recall data sourced from openFDA.gov.

How we calculate these metrics →