FDA Recall United States Ongoing 2026 recordClass II
Imu-Tek Animal Health, Incorporated
- Product
- Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally…
- Published
- April 8, 2026
- Distribution
- Product distributed in the following sta…
Imu-Tek Animal Health, Incorporated Recall: Product is potentially under-processed.
United States
OngoingClass II
- Company
- Imu-Tek Animal Health, Incorporated
- Product
- Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day…
- Recall date
- February 24, 2026
- Source
- FDA
Reason for recall
Product is potentially under-processed.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band seal, 500 mg capsule, 7 38654 00026 7, Imu-Tek, Inc. Ft. Collins, CO 80524. | Not published in this source record | 1003 botlles | Lot #013, 092826 Expiration |
Distribution
- Product distributed in the following states: AK
- AL
- AZ
- CA
- CO
- CT
- FL
- HI
- IA
- ID
- IL
- IN
- MA
- MD
- MO
- MS
- NC
- NE
- NH
- NV
- NY
- OK
- OR
- SC
- TN
- TX
- UT
- WA
- WI
- WY.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0660-2026
- Event ID
- 98486
- Status
- Ongoing
- Classification
- Class II
- Company
- Imu-Tek Animal Health, Incorporated
- Product description
- Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band seal, 500 mg capsule, 7 38654 00026 7, Imu-Tek, Inc. Ft. Collins, CO 80524.
- Quantity
- 1003 botlles
- Reason
- Product is potentially under-processed.
- Recall initiation date
- February 24, 2026
- Report date
- April 8, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Product distributed in the following states: AK, AL, AZ, CA, CO, CT, FL, HI, IA, ID, IL, IN, MA, MD, MO, MS, NC, NE, NH, NV, NY, OK, OR, SC, TN, TX, UT, WA, WI, WY.
- UPC, lot, and code information
- Lot #013, 092826 Expiration
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 98486 with 1 other product entry in Public Health Trace.
Responsible company: Imu-Tek Animal Health, Incorporated
Other recalls from Imu-Tek Animal Health, Incorporated
FDA Recall United States Ongoing 2026 recordClass II
Imu-Tek Animal Health, Incorporated
- Product
- Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally…
- Published
- April 8, 2026
- Distribution
- Product distributed in the following sta…
FDA Recall United States Ongoing 2026 recordClass II
Imu-Tek Animal Health, Incorporated
- Product
- Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Die…
- Published
- February 11, 2026
- Distribution
- Distributed in : AZ, CA, CO, FL, MA, ME,…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alaska | 1 |
| Alabama | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Hawaii | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| New Hampshire | 1 |
| Nevada | 1 |
| New York | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
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.
