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LYMA LIFE

⚠️ High Risk

FEI: 3022680300 • Swindon • UNITED KINGDOM

FEI

FEI Number

3022680300

📍

Location

Swindon

🇬🇧
🏢

Address

Hillmead Drive 9, , Swindon, , United Kingdom

High Risk

FDA Import Risk Assessment

57.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

14
Total Refusals
6
Unique Violations
11/8/2023
Latest Refusal
11/1/2022
Earliest Refusal

Score Breakdown

Violation Severity
57.0×40%
Refusal Volume
43.6×30%
Recency
56.5×20%
Frequency
100.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

47612×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

2239×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

2782×

NO TAG

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).

472×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

2561×

INCONSPICU

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

Refusal History

DateProductViolationsDivision
11/8/2023
54FCY94ASHWAGANDHA (HERBAL & BOTANICALS, NOT TEAS)
256INCONSPICU
Division of Northern Border Imports (DNBI)
1/12/2023
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
476NO REGISTR
Division of Southeast Imports (DSEI)
11/29/2022
79OLPOVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
260FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/16/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/16/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/16/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/16/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/16/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/16/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/16/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)
11/10/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
278NO TAG
47NON STD
476NO REGISTR
Division of Southeast Imports (DSEI)
11/8/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
278NO TAG
47NON STD
476NO REGISTR
Division of Southeast Imports (DSEI)
11/8/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
Division of Southeast Imports (DSEI)
11/1/2022
79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION
223FALSE
476NO REGISTR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LYMA LIFE's FDA import refusal history?

LYMA LIFE (FEI: 3022680300) has 14 FDA import refusal record(s) in our database, spanning from 11/1/2022 to 11/8/2023.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. LYMA LIFE's FEI number is 3022680300.

What types of violations has LYMA LIFE received?

LYMA LIFE has been cited for 6 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about LYMA LIFE come from?

All FDA import refusal data for LYMA LIFE is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.