Update on Guidance on Reporting COVID-19 Vaccines
Texas Health and Human Services Commission sent this bulletin at 12/14/2023 08:15 AM CST / Este e-mail ha sido enviado por Texas Health and Human Services Commission el 12/14/2023 08:15 AM CST|
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Overview:
Providers can no longer report de-authorized COVID-19 vaccines in ImmTrac2 and will now receive an error message upon attempting to do so. Please share this communication with your IT staff and Electronic Health Record vendors for their awareness.
Update on Reporting COVID-19 Vaccines in ImmTrac2:
In 2023 the Food and Drug Administrations (FDA) de-authorized some COVID-19 vaccines. The expiration date for these COVID-19 vaccines is listed in the table below. Providers can no longer report administration of COVID-19 vaccines (new or historical) after their end date in ImmTrac2.
Unauthorized trade names and corresponding end dates in ImmTrac2:
|
Tradename |
CVX Code |
CPT Code |
End Date |
|
Pfizer COVID-19 Vaccine |
208 |
91300 |
4/18/2023 |
|
Spikevax 100mcg/0.5mL |
207 |
- |
4/18/2023 |
|
Moderna COVID-19 Vaccine |
207 |
91301 and 91306 |
4/18/2023 |
|
COMIRNATY TS, 30mcg/0.3mL |
217 |
91305 |
4/18/2023 |
|
COMIRNATY TS, 10mcg/0.2mL |
218 |
91307 |
4/18/2023 |
|
COMIRNATY TS, 3mcg/0.2mL |
219 |
91308 |
4/18/2023 |
|
Moderna COVID-19 Pedi 6-11yrs) |
221 |
91309 |
4/18/2023 |
|
Moderna COVID-19 Pedi (6mos-5yrs) |
228 |
91311 |
4/18/2023 |
|
Janssen COVID-19 Vaccine |
212 |
91303 |
6/20/2023 |
|
Moderna Bivalent |
229 |
91313 and 91314 |
9/11/2023 |
|
Moderna Bivalent Booster (6mos-5yrs) |
230 |
91316 |
9/11/2023 |
|
Pfizer bivalent 12+ |
300 |
91312 |
9/11/2023 |
|
Pfizer Bivalent Peds (5-11yrs) |
301 |
91315 |
9/11/2023 |
|
Pfizer Bivalent Booster (6mos-4yrs) |
302 |
- |
9/11/2023 |
|
Novavax COVID-19 Vaccine |
211 |
91304 |
10/3/2023 |
Currently authorized tradenames accepted in ImmTrac2:
|
Tradename |
CVX Code |
CPT Code |
|
Pfizer (6mos-4yrs) (2023-24 Formula) |
308 |
91318 |
|
Pfizer (5-11yrs) (2023-24 Formula) |
310 |
91319 |
|
Comirnaty 12+(2023-24 Formula) |
309 |
91320 |
|
Moderna (6mos-11yrs) (2023-24 Formula) |
311 |
91321 |
|
Spikevax 12+ (2023-24 Formula) |
312 |
91322 |
|
Novavax 12+ (2023-24 Formula) |
313 |
91304 |
Impact of the Change:
A. Providers reporting through ImmTrac2 user interface:
If a provider reports administration of a COVID-19 vaccine after the vaccine end date, they will receive a warning message and the immunization will not be accepted. See Figure 1.

Figure 1: Display of warning message “Validation Errors”
B. Providers reporting through data exchange:
If a provider reports administration of a COVID-19 vaccine after the vaccine end date, they will receive the following rejection errors:
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For COVID-19 Monovalent vaccines revoked on April 18, 2023:
IMR-139::Record rejected. Invalid administration date. This vaccine (Vaccine Name: COVID-19 mRNA, LNP-S, bival, PF,50mcg/0.5 mL) is not authorized for administration by FDA after Mon Sep 11 00:00:00 CDT 2023. -
For COVID-19 Bivalent vaccines revoked on September 11, 2023:
IMR-139::Record rejected. Invalid administration date. This vaccine (Vaccine Name: COVID-19 mRNA, LNP-S, bival, PF,50mcg/0.5 mL) is not authorized for administration by FDA after Mon Sep 11 00:00:00 CDT 2023.
Questions?
For questions related to this communication, contact:
- Online related – ImmTrac2@dshs.texas.gov or 800-348-9158, Option 1
- Data exchange related –ImmTracMU@dshs.texas.gov or 800-348-9158, Option 3
