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Pacific Health Sciences Llc Recall: Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate

United States

OngoingClass II

Company
Pacific Health Sciences Llc
Product
Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptid…
Recall date
September 14, 2026
Source
FDA

Reason for recall

Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptides, All-Natural Aid for Strengthening Hair, Skin, Nails, Muscles & Joints, 180 Veggie Capsules. UPC: none Not published in this source record 395 units 25009CP

Distribution

  • Product is primarily distributed to private practice medical offices in California
  • Oregon
  • Washington
  • Kentucky
  • Massachusetts
  • and Hawaii

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-1401-2026
Event ID
99897
Status
Ongoing
Classification
Class II
Company
Pacific Health Sciences Llc
Product description
Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptides, All-Natural Aid for Strengthening Hair, Skin, Nails, Muscles & Joints, 180 Veggie Capsules. UPC: none
Quantity
395 units
Reason
Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate
Recall initiation date
September 14, 2026
Report date
October 7, 2026
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
Product is primarily distributed to private practice medical offices in California, Oregon, Washington, Kentucky, Massachusetts, and Hawaii
UPC, lot, and code information
25009CP
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Pacific Health Sciences Llc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.