Signature Breads, Inc.

Complete recall history across all FDA and CPSC categories — 10 total recalls

Signature Breads, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (10)

FDA food safety enforcement actions by Signature Breads, Inc.

Date Product Reason Class
Dec 20, 2015 Signature Breads Frozen Parbaked French Dinner Rolls 22251; 280 Units - 1 OZ,... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked Assorted Petit Pain 22032; 144 UNITS - 1.75 ... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked French Sub Roll 22201, 72 UNITS - 3.25 OZ, N... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked French Dinner Roll 22245; 120 units - 1.25 O... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked French Mini Baguette 22205; 48 UNITS - 5 OZ,... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked Assorted Dinner Rolls 22213; 240 UNITS - NET... Product may contain metal fragments. Class II
Dec 20, 2015 Piantedosi French Dinner rolls C-301, Signature Breads French Dinner Rolls 22... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked French Petit Pain 22203, 144 UNITS - 1.75 OZ... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked French Sub Grande 22089; 36 UNITS - 5.9 OZ, ... Product may contain metal fragments. Class II
Dec 20, 2015 Signature Breads Frozen Parbaked Baguette 22202, 25 UNITS - 8.75 OZ, NET WT. ... Product may contain metal fragments. Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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