Apollo Care 503B outsourcing facility · Columbia, MO

This is a record of what FDA published, not a rating. Last FDA inspection and Form 483 status below are as published in FDA's registered outsourcing facilities table (as of Sep 30, 2026).

FDA registration record

Listed by FDA asApollo Care, Columbia, MO
City / stateColumbia, MO
FDA's table lists city and state only, not a street address.
Contact phone (as listed by FDA)573-441-8900
Initial registration date9/14/2017
Most recent registration date12/24/2025
Outsourcing facilities must re-register annually (Oct 1 – Dec 31) to remain on FDA's list.
Last inspection (FDA table)7/28/2026
Form 483 issued at last inspection?Yes
Recall conducted? (FDA table)No
Action based on last inspectionOpen
“Open” means FDA has not determined whether further action will be taken (per FDA's table notes).
Intends to compound sterile drugs from bulk substancesYes
Self-reported by the facility at registration; FDA notes this information has not been verified by FDA.
Prior compounding inspection history flagYes
FDA footnotes this facility as the subject of at least one previous compounding inspection that resulted in a Form 483, warning letter or other action.

Source: FDA Registered Outsourcing Facilities

Published FDA records

4Form 483 records
2Warning letters
7Recall events (openFDA)
0Uncertain-match items

Counts include only items from FDA's table or exact name + city + state matches. They are counts of published records, not a score. Uncertain matches are shown below but not counted.

State board of pharmacy license lookup

Missouri Division of Professional Registration Licensee Search (Board of Pharmacy) (license lookup)

Search the state board's lookup for this facility's license status and any disciplinary actions. We link to the state-level tool only and do not list license numbers. FDA's table does not include state board actions. Facilities that ship across state lines may also hold non-resident licenses in your state, so check your own state's board too.

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Timeline of FDA actions

Newest first. Sources: FDA's registration table, FDA's compounding actions page (2019 onward on the live page), and openFDA drug enforcement records. Items marked Uncertain match may relate to a different site or entity and are not counted. How matching works.

  1. Recall Matched
    Recall event 99505
    Class II · Ongoing · 11 product line(s) · Recall no. D-0747-2026, D-0748-2026, D-0749-2026, D-0750-2026, D-0751-2026, D-0752-2026 …
    Recalling firm as listed: Apollo Care, LLC, Columbia, MO. Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
    openFDA record · openFDA drug enforcement API
  2. Inspection FDA table
    Last inspection per FDA table; Form 483 issued: Yes
    No document link published · FDA registered outsourcing facilities table
  3. Form FDA 483 FDA table
    Form FDA 483 issued, per FDA's registration table; document link from FDA's compounding actions page ("483 Issued 07/28/2026 (PDF - 1.60MB)")
    FDA document · FDA registered outsourcing facilities table
  4. Warning letter Matched
    Warning Letter (02/02/2026)
    Listed on FDA page under: Apollo Care LLC, Columbia, MO - 503B Facility
    FDA document · FDA Compounding: Inspections, Recalls, and other Actions
  5. Recall Matched
    Recall event 96754
    Class II · Ongoing · 1 product line(s) · Recall no. D-0409-2025
    Recalling firm as listed: Apollo Care, LLC, Columbia, MO. Reason: Lack of Assurance of Sterility
    openFDA record · openFDA drug enforcement API
  6. Form FDA 483 Matched
    483 Issued 03/27/2025 (PDF - 2 MB)
    Listed on FDA page under: Apollo Care LLC, Columbia, MO - 503B Facility
    FDA document · FDA Compounding: Inspections, Recalls, and other Actions
  7. Regulatory meeting Matched
    Regulatory Meeting Held 11/27/2023
    Listed on FDA page under: Apollo Care LLC, Columbia, MO - 503B Facility
    No document link published · FDA Compounding: Inspections, Recalls, and other Actions
  8. Recall Matched
    Recall event 92348
    Class II · Ongoing · 16 product line(s) · Recall no. D-0632-2023, D-0633-2023, D-0634-2023, D-0635-2023, D-0636-2023, D-0637-2023 …
    Recalling firm as listed: Apollo Care, LLC, Columbia, MO. Reason: Lack of Assurance of Sterility
    openFDA record · openFDA drug enforcement API
  9. Form FDA 483 Matched
    483 Issued 04/05/2023 (PDF - 2 MB)
    Listed on FDA page under: Apollo Care LLC, Columbia, MO - 503B Facility
    FDA document · FDA Compounding: Inspections, Recalls, and other Actions
  10. Recall Matched
    Recall event 91674
    Class II · Ongoing · 1 product line(s) · Recall no. D-0487-2023
    Recalling firm as listed: Apollo Care, Columbia, MO. Reason: Lack of assurance of sterility: Suspected microbial growth present on external label packaging.
    openFDA record · openFDA drug enforcement API
  11. Recall Matched
    Recall event 89011
    Class II · Terminated · 1 product line(s) · Recall no. D-0277-2022
    Recalling firm as listed: Apollo Care, Columbia, MO. Reason: Crystallization: Product appears to be turbid.
    openFDA record · openFDA drug enforcement API
  12. Form FDA 483 Matched
    483 Issued 09/8/2021 (PDF - 2 MB)
    Listed on FDA page under: Apollo Care LLC, Columbia, MO - 503B Facility
    FDA document · FDA Compounding: Inspections, Recalls, and other Actions
  13. Warning letter Matched
    Warning Letter (03/20/2019)
    Listed on FDA page under: Apollo Care LLC, Columbia, MO - 503B Facility
    FDA document · FDA Compounding: Inspections, Recalls, and other Actions
  14. Recall Matched
    Recall event 79517
    Class II · Terminated · 2 product line(s) · Recall no. D-0614-2018, D-0615-2018
    Recalling firm as listed: Apollo Care, Columbia, MO. Reason: Stability Data Does Not Support Expiry: 90-day beyond use date (BUD) for the affected product is not supported.
    openFDA record · openFDA drug enforcement API
  15. Recall Matched
    Recall event 79331
    Class II · Terminated · 2 product line(s) · Recall no. D-0579-2018, D-0580-2018
    Recalling firm as listed: Apollo Care, Columbia, MO. Reason: Stability Data Does Not Support Expiry: 90-day beyond use date (BUD) for the affected product is not supported.
    openFDA record · openFDA drug enforcement API