Class IIOngoing · reported 2025-12-31

First & Last Tavern Puttanesca Sauce (olives, capers, hot peppers) 26 FL OZ (1 lb, 10…

First & Last Tavern recalled this product and the FDA reported the enforcement action on 31 December 2025 as Class II. The recall was initiated by the firm. May be contaminated with Clostridium botulinum

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product
First & Last Tavern Puttanesca Sauce (olives, capers, hot peppers) 26 FL OZ (1 lb, 10 oz) 737g
Reason for recall
May be contaminated with Clostridium botulinum
Recalling firm
First & Last Tavern
Firm location
Hartford, Connecticut, United States
Classification
Class II
Status
Ongoing
Recall number
H-0336-2026
Quantity
30 cases
Distribution
CT, MA
Initiated
31 October 2025
Reported by FDA
31 December 2025
Firm notified by
Press Release
Product codes
Expiration/Use By: 09/26

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
  • The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
  • This is one of 3 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 3 separate recalls, which almost every published figure does, overstates it by a factor of 3. All 3 of them are listed on this page.
  • This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
  • The distribution pattern names 2 states, and the FDA published the enforcement report 2 months after the firm began the recall.
  • Sauces and dips sit at the intersection of the acidified foods rule and the allergen rule: an equilibrium pH above 4.6 turns a shelf-stable product into a botulism risk, and the ingredient list is long enough that an allergen is easy to lose.

Named in the distribution pattern: Connecticut, Massachusetts. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.

What this recall was for

Clostridium botulinum

Clostridium botulinum recalls are recalls of the process, not of a test result: the organism produces its toxin without oxygen, so a low-acid food in a sealed container that missed its scheduled process is recalled whether or not toxin was ever found.

A preventive controls plan covers a botulism risk under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 113
Thermally processed low-acid foods in hermetically sealed containers: the scheduled process, its establishment by a competent authority, and the records proving every container received it.
21 CFR 108.35
Emergency permit control: the registration and process filing a low-acid canned food processor must hold before it may operate.

Filed under sauces, dips and condiments. A product can sit in more than one.

Every product in this recall

The FDA opened 3 enforcement records for this one recall, one per product code. This page carries all of them; the 2 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.

The other 2 records of FDA event 97906
ReportedProductFirmReasonClass
2025-12-31First & Last Tavern Marinara Sauce (tomato & basil) 26 FL OZ (1 lb, 10 oz) 737gFirst & Last TavernMay be contaminated with Clostridium botulinumClass II
2025-12-31First & Last Tavern Traditional Pasta Sauce (meat flavored) 26 FL OZ (1 lb., 10 oz) 737gFirst & Last TavernMay be contaminated with Clostridium botulinumClass II

Other sauces, dips and condiments recalls for the same reason

These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.

ReportedProductFirmReasonClass
2025-12-31First & Last Tavern Marinara Sauce (tomato & basil) 26 FL OZ (1 lb, 10 oz) 737gFirst & Last TavernMay be contaminated with Clostridium botulinumClass II
2025-12-31First & Last Tavern Traditional Pasta Sauce (meat flavored) 26 FL OZ (1 lb., 10 oz) 737gFirst & Last TavernMay be contaminated with Clostridium botulinumClass II
2024-04-10AJI MORI***CHILLIMAMI SAUCE***UMAMI BOMB***NET WT. 250ml. Packaged in a LDPE bottle. Refrigerate after opening.AJI MORI SAUCE CORPPotential contamination with Clostridium botulinumClass II
2022-09-07Lyons Ready Care Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Grade A Made with 2% Milk Fat Milk, Vitamins A & D Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 45796-10044 2. Item 10044. 24 count case UPC 10045796100449. 2. 32 FL OZ (1 QT) 946mL UPC 0 45796-10046 6. Item 10046. 12 count case UPC 10045796100463. Refrigerate after opening. Manufactured for Lyons Magnus, Fresno, CA 93702.Lyons Magnus, IncFindings and potential for Cronobacter sakazakii and Clostridium botulinum.Class I
2022-09-07Chocolate Syrup, MIDRWB36XX. Item 10137 Ingredients: water, cocoa (processed with alkali), cane sugar. Net: 235 gal (889.6L) Lyons Magnus Fresno, CA 93702Lyons Magnus, IncFindings and potential for Cronobacter sakazakii and Clostridium botulinum.Class I
2022-09-07Sysco Imperial Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Made with Grade A 2% Fat Milk, Vitamins A & D. Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 74865-94550 9. Reorder # 0429357. 24 count case UPC 10074865945506. 2. 32 FL OZ (1 QT) 946mL UPC 7 34730-55614 7. Reorder # 4254296. 12 count case UPC 10734730556144. Refrigerate prior to serving. Shake well. Distributed by Sysco Corporation, Houston, Texas 77077.Lyons Magnus, IncFindings and potential for Cronobacter sakazakii and Clostridium botulinum.Class I
2018-08-15Taco Bell Salsa Con Queso Mild 15oz retail jar UPC 21000024490 packaged in 12 count and 8 count casesKRAFT HEINZ FOODS COMPANYProduct is at risk for growth of Clostridium botulinumClass II
2017-05-03Shrimp Satay Hot Dry Shrimp-Chili Sauce, Net: 6 and 9oz , 12 units/caseTP Food Processing Inc.TP Food Processing, Inc. is recalling Lemongrass Satay and Shrimp Satay because the acidified sauces were not properly produced making them susceptible to contamination with Clostridium botulinum.Class II

Other records from First & Last Tavern

The FDA opens one enforcement record per product code, so several of these are frequently one recall event.

ReportedProductFirmReasonClass
2025-12-31First & Last Tavern Marinara Sauce (tomato & basil) 26 FL OZ (1 lb, 10 oz) 737gFirst & Last TavernMay be contaminated with Clostridium botulinumClass II
2025-12-31First & Last Tavern Traditional Pasta Sauce (meat flavored) 26 FL OZ (1 lb., 10 oz) 737gFirst & Last TavernMay be contaminated with Clostridium botulinumClass II

All 3 records for First & Last Tavern

All 2025 recalls · All FDA food recall data

21 CFR 113 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.