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life spring mfg ltd

FDA import alert and refusal historyNorth Vancouver, CanadaFEI 3002332300

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Example subjectlife spring mfg lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, life spring mfg ltd (North Vancouver, Canada) is on the red list of FDA Import Alert 99-38 (Low-acid canned/acidified foods: inadequate process control) for respiractin for children; respiractin, published by FDA on December 1, 2023, and has 9 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
IA 99-38 · red list
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NO PROCESS
Last warning letter
None found
Last inspection
None on record

Every FDA record for life spring mfg ltd

10 records, newest first. Each line links to the FDA page it came from.

2024

  1. Import refusal
    Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO PROCESSEntry MK8-5891275-3Show 2 lines
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO PROCESSEntry MK8-5891275-3Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO PROCESSEntry MK8-5891275-3Source
    Source

2023

  1. Import alert listing
    Listed on Import Alert 99-38red listRespirActin for Children; RespirActin
    Source
  2. Import refusal
    Refused, 3 lines in one entry: Herbals & botanicals (not teas), n.e.c.NEEDS FCENO PROCESSEntry MK8-5826839-6Show 3 lines
    Source

2018

  1. Import refusal
    Refused, 4 lines in one entry: Mineral n.e.c.NUTRIT LBLEntry MK8-5333738-6Show 4 lines
    Source

Refusal charges, in plain English

  • NO PROCESS5 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • NUTRIT LBL4 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • NEEDS FCE3 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

Questions about life spring mfg ltd

Is life spring mfg ltd on an FDA import alert?
Yes. As of October 26, 2026, life spring mfg ltd is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for respiractin for children; respiractin; FDA published the listing on December 1, 2023.
Has FDA refused shipments from life spring mfg ltd?
Yes. FDA refused 9 shipment lines from life spring mfg ltd between May 23, 2018 and April 16, 2024. The most recent, on April 16, 2024, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse life spring mfg ltd's shipments?
The most frequent charges are NO PROCESS (no scheduled process filed, 5 lines) and NUTRIT LBL (nutrition information missing from label, 4 lines).
What is life spring mfg ltd's FEI number?
life spring mfg ltd's FDA Establishment Identifier (FEI) is 3002332300.
Can shipments from life spring mfg ltd still enter the U.S.?
Shipments of respiractin for children; respiractin from life spring mfg ltd can be detained without physical examination under Import Alert 99-38; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectlife spring mfg lt added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.