RECALL RECORD — CLASS IIRecall closedF1583-2013/FDA enforcement

"***Dietary Supplement 4hb Stack Bedtime***52 Caplets***manufactured Exclusively for: Kirkland…

What you need to know

Class II
  • What happened

    Customer reported that a product user complained that the caplets were not coated, making them difficult to swallow.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAIN, WAMore supplements

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Product identification

Source: FDA FOOD

Brand nameFlorida Nutri Labs, LLC
Recalling firmFlorida Nutri Labs, LLCLakeland, FL, United States
UPC / barcodes
0 13964 66251 1
Lot / date codes
  • Lot #12-194, expiration date 12/2014 UPC #0 13964 66251 1
Distribution area
INWA

Product was distributed to 1 distributor, Kirland Science Labs located in Seattle, WA.

United States

Quantity affected2526 bottles
Recall initiationFDA report date: July 10, 2013
FDA recall numberF1583-2013

Beyond the headline

The recall, in context

Florida Nutri Labs, LLC initiated this supplements recall on May 22, 2013. The FDA enforcement report states: Customer reported that a product user complained that the caplets were not coated, making them difficult to swallow. The FDA report lists distribution as: Product was distributed to 1 distributor, Kirland Science Labs located in Seattle, WA.

The FDA enforcement report describes the reason as: Customer reported that a product user complained that the caplets were not coated, making them difficult to swallow.

"***Dietary Supplement 4hb Stack Bedtime***52 Caplets***manufactured Exclusively for: Kirkland… was made or distributed by Florida Nutri Labs, LLC in Lakeland, FL, United States. This page reflects FDA report F1583-2013, dated July 10, 2013.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the "***Dietary Supplement 4hb Stack Bedtime***52 Caplets***manufactured Exclusively for: Kirkland… recall?

Florida Nutri Labs, LLC recalled "***Dietary Supplement 4hb Stack Bedtime***52 Caplets***manufactured Exclusively for: Kirkland… in an FDA Class II enforcement action reported as F1583-2013. Customer reported that a product user complained that the caplets were not coated, making them difficult to swallow.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Florida Nutri Labs, LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F1583-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.