Skip to main content

Loffredo Fresh Gardens Inc. DBA Produce Innovations Recall: An ingredient in yogurt contains soy lecithin, but soy is not declared on the label.

United States

TerminatedClass II

Company
Loffredo Fresh Gardens Inc. DBA Produce Innovations
Product
Your Way Fresh, Greek Yogurt + Peach Parfait; Net wt. 6.25 o…
Recall date
August 19, 2021
Terminated
September 14, 2021
Source
FDA

Reason for recall

An ingredient in yogurt contains soy lecithin, but soy is not declared on the label.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Your Way Fresh, Greek Yogurt + Peach Parfait; Net wt. 6.25 oz (177 g); UPC 8 54426 00809 2; Distributed by Your Way Fresh, Newport Beach, CA, 12 cups per case; Not published in this source record 28 cases lot code 21229 and 21230.

Distribution

  • Distributed to retail stores in IA
  • IN
  • MO
  • MN
  • NE
  • OK
  • and TX.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0905-2021
Event ID
88538
Status
Terminated
Classification
Class II
Company
Loffredo Fresh Gardens Inc. DBA Produce Innovations
Product description
Your Way Fresh, Greek Yogurt + Peach Parfait; Net wt. 6.25 oz (177 g); UPC 8 54426 00809 2; Distributed by Your Way Fresh, Newport Beach, CA, 12 cups per case;
Quantity
28 cases
Reason
An ingredient in yogurt contains soy lecithin, but soy is not declared on the label.
Recall initiation date
August 19, 2021
Report date
September 8, 2021
Classification date
Not published in this source record
Termination date
September 14, 2021
Distribution pattern
Distributed to retail stores in IA, IN, MO, MN, NE, OK, and TX.
UPC, lot, and code information
lot code 21229 and 21230.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 88538 with 2 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Loffredo Fresh Gardens Inc. DBA Produce Innovations

Product
Your Way Fresh, Sliced Banana + Strawberry Yogurt Parfait; N…
Published
September 8, 2021
Distribution
Distributed to retail stores in IA, IN,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Loffredo Fresh Gardens Inc. DBA Produce Innovations

Product
Strawberry Yogurt Granola Parfait packaged in clear plastic…
Published
September 8, 2021
Distribution
Distributed to retail stores in IA, IN,…

View recall →

Responsible company: Loffredo Fresh Gardens Inc. DBA Produce Innovations

Other recalls from Loffredo Fresh Gardens Inc. DBA Produce Innovations

FDA Recall United States Terminated Historical recordClass II

Loffredo Fresh Gardens Inc. DBA Produce Innovations

Product
Your Way Fresh, Sliced Banana + Strawberry Yogurt Parfait; N…
Published
September 8, 2021
Distribution
Distributed to retail stores in IA, IN,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Loffredo Fresh Gardens Inc. DBA Produce Innovations

Product
Strawberry Yogurt Granola Parfait packaged in clear plastic…
Published
September 8, 2021
Distribution
Distributed to retail stores in IA, IN,…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Iowa 1
Indiana 1
Missouri 1
Minnesota 1
Nebraska 1
Oklahoma 1
Texas 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.