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Class I: serious health riskTerminated

Standard Homeopathic Hyland's Baby Nighttime Teething Tablets Recall

Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS (0

Standard Homeopathic Company · Los Angeles, CA

Risk level
Class I
Reported by FDA
May 31, 2017
Recall ID
D-0864-2017
Check your lot numberHow we source this data

Summary

Standard Homeopathic recalled Hyland's Baby Nighttime Teething Tablets starting Apr 13, 2017. The FDA classified it as Class I (serious health risk) and published enforcement report D-0864-2017 on May 31, 2017. Reason: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels. Status: Terminated.

Why it was recalled

Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.

Product description

Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS (0.0000000000003% alkaloids, calculated), Calcarea Phosphorica 6X HPUS, Chamomilla 6X HPUS, Coffea Cruda 6X HPUS, Magnesia Phosphorica 6X HPUS, Rheum 6X HPUS, Silicea 12X HPUS] Quick-Dissolving Tablets, 135-count bottle, Manufactured for: Hyland's, Inc., Los Angesles, CA 90061, NDC 54973-3197-1, UPC 3 54973 31971 4.

Lot numbers, UPCs & expiration codes

All lots within expiry

Where it was sold

Nationwide in the USA and Puerto Rico.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0864-2017
Classification
Class I
Status
Terminated
Recall initiated
Apr 13, 2017
FDA report date
May 31, 2017
Quantity
692,115 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Standard Homeopathic Company

Original FDA data

Every field from FDA enforcement report D-0864-2017, exactly as published.

Show all FDA fields
City
Los Angeles
State
CA
Status
Terminated
Country
United States
Event ID
77009
Address
154 W 131st St
Code information
All lots within expiry
Postal code
90061-1616
Report date
May 31, 2017
Product type
Drugs
Recall number
D-0864-2017
Classification
Class I
Recalling firm
Standard Homeopathic Company
Product quantity
692,115 bottles
Termination date
Oct 26, 2017
Reason for recall
Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS (0.0000000000003% alkaloids, calculated), Calcarea Phosphorica 6X HPUS, Chamomilla 6X HPUS, Coffea Cruda 6X HPUS, Magnesia Phosphorica 6X HPUS, Rheum 6X HPUS, Silicea 12X HPUS] Quick-Dissolving Tablets, 135-count bottle, Manufactured for: Hyland's, Inc., Los Angesles, CA 90061, NDC 54973-3197-1, UPC 3 54973 31971 4.
Distribution pattern
Nationwide in the USA and Puerto Rico.
Recall initiation date
Apr 13, 2017
Initial firm notification
Press Release
Center classification date
May 24, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0864-2017, published May 31, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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