CLASS I Food recall · Reported 22 Nov 2017 · FDA Enforcement Report

Texas Roadhouse Barbecue Sauce, NET, Mfg. exclusively recalled

CFS West Holdings is recalling Texas Roadhouse Barbecue Sauce, NET, Mfg. exclusively for: Texas Roadhouse Restaurants, distributed in 12 states. The recall was initiated on 31 Oct 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes17285SS
Quantity recalled908 cases total

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0367-2018
FDA event ID
78420
Recalling firm
CFS West Holdings, New Century, KS
Classification
Class I
Status
Terminated
Recall initiated
31 Oct 2017
FDA classified
21 Nov 2017
Reported
22 Nov 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Egg
Product category
Sauces & Condiments

Timeline

31 Oct 2017Recall initiated by company
21 Nov 2017Classified by FDA+21 days
22 Nov 2017Published in enforcement report+1 day

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Products potentially contain undeclared egg.

Product as listed by the FDA

Texas Roadhouse Barbecue Sauce, NET 3/2 gallon, Mfg. exclusively for: Texas Roadhouse Restaurants, Louisville, KY, packaged in plastic pouches.

Where it was distributed

Product distributed to distributors in AR, CO, IA, IL, KS, KY, LA, MI, MO, MN, MS, and ND

ArkansasColoradoIowaIllinoisKansasKentuckyLouisianaMichiganMinnesotaMissouriMississippiNorth Dakota

Questions about this recall

Why was it recalled?

Products potentially contain undeclared egg.

Which lots are affected?

17285SS

Where was it sold?

Product distributed to distributors in AR, CO, IA, IL, KS, KY, LA, MI, MO, MN, MS, and ND

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 78420

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