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Upspring,Ltd FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Upspring,Ltd has 1 FDA recall (1 Class I), 2 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Upspring,Ltd, the most recent on Apr 6, 2012.

What these totals cover: FDA records filed under the name "Upspring,Ltd" and its spelling variant "Upspring".

Latest recall: F-1149-2020 · Class I · Jul 23, 2020
Latest inspection: Apr 8, 2025 · NAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	1 (1 Class I)	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	2	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Upspring,Ltd's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	Recall records	Class I
2026	0	0	0
2025	1	0	0
2024	0	0	0
2023	0	0	0
2022	0	0	0
2021	1	0	0
2020	0	1	1
2019	0	0	0
2018	0	0	0
2017	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Upspring,Ltd FDA Warning Letters

1 warning letter on Apr 6, 2012.

Issued	Subject	Issuing office	Close-out letter
Apr 6, 2012

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent recalls

1 recall record on Jul 23, 2020.

Number	Class	Product	Date
F-1149-2020	Class I	UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Promotes nutrition For Healthy Growth + Immune…	Jul 23, 2020

Recent FDA inspections

2 inspections from Nov 19, 2021 to Apr 8, 2025.

Date	Site	Product	Classification	FEI
Apr 8, 2025	Austin, TX	Food/Cosmetics	No Action Indicated (NAI)	3007051926
Nov 19, 2021	Austin, TX	Food/Cosmetics	Voluntary Action Indicated (VAI)	3007051926

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Upspring,Ltd: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Apr 6, 2012.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3007051926	Austin, TX	2	Apr 8, 2025

Upspring,Ltd and the FDA: common questions

Has Upspring,Ltd received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Upspring,Ltd. The most recent is dated Apr 6, 2012.

Has Upspring,Ltd received an FDA Form 483?

FDA has not published a Form 483 for "Upspring,Ltd" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Upspring,Ltd?

The most recent FDA inspection on file ended Apr 8, 2025 at Austin, TX and was classified NAI. FDA has 2 inspections of Upspring,Ltd on file.

Has Upspring,Ltd had an FDA recall?

Yes. Upspring,Ltd has 1 FDA recall on record, 1 of them Class I, the most serious class. The most recent started Jul 23, 2020.

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