CLASS III Food recall · Reported 25 Jan 2017 · FDA Enforcement Report

Starkey Spring Water recalled by Starkey Water

Starkey Water is recalling Starkey Spring Water, distributed in Colorado, Florida, Iowa, Pennsylvania, Texas. The recall was initiated on 4 Jan 2017 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesProduced On 11/26/14
Quantity recalled300 cases (15 bottles per case)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1333-2017
FDA event ID
76172
Recalling firm
Starkey Water, Council, ID
Brand
Starkey
Classification
Class III
Status
Terminated
Recall initiated
4 Jan 2017
FDA classified
19 Jan 2017
Reported
25 Jan 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Lead & Heavy Metals
Product category
Bottled Water

Timeline

4 Jan 2017Recall initiated by company
19 Jan 2017Classified by FDA+15 days
25 Jan 2017Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

12 ppb of arsenic was detected in water sample

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

Starkey Spring Water, 16.9 FL oz. (500 mL) glass bottle. packed 15 bottles in cardboard box. Product UPC 8 11904 02000 7. Case UPC 8 11904 02002 1.

Where it was distributed

distributed in CO, FL, IA, PA, and TX.

ColoradoFloridaIowaPennsylvaniaTexas

Questions about this recall

Why was it recalled?

12 ppb of arsenic was detected in water sample

Which lots are affected?

Produced On 11/26/14

Where was it sold?

distributed in CO, FL, IA, PA, and TX.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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