Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Vitony Bakery, Inc.

Vitony Bakery, Inc. Recalls

All product recalls associated with Vitony Bakery, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

726

Class I (Serious)

175

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 4241–4260 of 11124 recalls

Brazo Gitano Guava Cheese Roll (Vitony Bakery) – Multiple Allergens (2019)

Failure to declare Soy, FD&C Yellow #5 and #6 and lack of Keep Refrigerated labeling.

Class IIModerate

FDAAug 9, 2019Nationwide• Vitony Bakery, Inc.

Bizcocho de Guayaba y Coco (Vitony Bakery) – Undeclared Sulfite (2019)

Failure to declare Sodium Metabisulfite.

Class IIModerate

FDAAug 9, 2019Nationwide• Vitony Bakery, Inc.

Radiometer AQURE System (Radiometer) – Patient Mix-Up Risk (2019)

The firm has become aware that there is a potential problem relating to the blood gas and immunoassay analyzer Systems that may result in patient mix-up when connected to some third-party devices. The error may lead to serious adverse health consequences for the patient caused by patient data mix-up.

1...211 212213214 215...557

Page 213 of 557Next

High

FDAAug 8, 2019Nationwide• Radiometer Medical ApS Akandevej 21 Bronshoj Denmark

Vivitrol Injection (Alkermes) – Incorrect Needle Labeling (2019)

Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch needles being placed in the 1 1/2 inch needle cardboard sleeve labelled as administration needles. The product vial is not impacted.

Class IIModerate

FDAAug 8, 2019Nationwide• Alkermes Inc

Clotrimazole Betamethasone Cream (Glenmark) – Temperature Abuse (2019)

Temperature Abuse: Complaints received of liquidy texture.

Class IIILow

FDAAug 7, 2019Nationwide• Glenmark Pharmaceuticals Inc., USA

Eptifibatide Injection (Akorn) – Short Fill Issue (2019)

Short Fill: fill volume was out of specification at 94 mL (specification: no less than 100 mL) and Failed Impurities/Degradation Specifications: Out of Specification (OOS) for known impurity, D-aspartic acid.

Class IIILow

FDAAug 6, 2019Nationwide• Akorn, Inc.

Eptifibatide Injection (Akorn) – Impurity Specifications (2019)

Failed Impurities/Degradation Specifications: Out of Specification (OOS) for known impurity, D-aspartic acid.

Class IIILow

FDAAug 6, 2019Nationwide• Akorn, Inc.

Eptifibatide Injection (Akorn) – Impurity Specifications (2019)

Failed Impurities/Degradation Specifications: Out of Specification (OOS) for known impurity, D-aspartic acid.

Class IIILow

FDAAug 6, 2019Nationwide• Akorn, Inc.

Broccoli Cheddar Bowl (Amy's) – Foreign Object Risk (2019)

Consumer complaints of black plastic found in product.

Class IIModerate

FDAAug 6, 2019CA, CO, CT +24 more• Amys Kitchen Inc

Lisinopril/HCTZ Tablets (RemedyRepack) – Foreign Tablet Presence (2019)

Presence of Foreign Tablets/Capsules: This is a spin-off recall of D-1581-2019 due to a product complaint where one of Lupin's Fenofibrate 145mg was observed in the 500 s count product bottle.

Class IIModerate

FDAAug 5, 2019PA• RemedyRepack Inc.

BD Jamshidi Bone Marrow Needle (Becton Dickinson) – Pouch Seal Defect (2019)

Product Pouches may not be sealed properly and compromise the sterility of the device

Low

FDAAug 1, 2019CA, IL• Becton Dickinson & Company

Stryker Chromophare Monitor Arm (Stryker) – Insufficient Weld (2019)

The mounts on the monitor may have an insufficient weld.

Low

FDAAug 1, 2019CA, CO, CT +18 more• Stryker Communications

Rocket Fetal Bladder Catheter (Rocket) – Device Kinking Risk (2019)

A complaint was received regarding kinking of the device prior to use. If a device is kinked it cannot be used. In addition, the company became aware that the device had been used for pleural drainage, which is not included in the device indications.

Moderate

FDAAug 1, 2019Nationwide• Rocket Medical Plc Industrial Estate Sedling Road Wear Indu Tyne & Wear Washington United Kingdom

GN Otometrics Leadwire (GN Otometrics) – Conductor Exposure (2019)

The electrode lead connector has a protruding conductor beyond insulation of approximately 0.1 mm.

High

FDAAug 1, 2019Nationwide• GN Otometrics Horskatten 9 Taastrup Denmark

Honey Lavender Tea (Milkweed & Monarch) – Salmonella Risk (2019)

Salmonella

recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas due to the potential for Salmonella contamination.

Class IIModerate

FDAAug 1, 2019CA, CO, FL +9 more• Milkweed & Monarch, LLC

Sandia Rose Tea (Milkweed & Monarch) – Salmonella Risk (2019)

Salmonella

recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas due to the potential for Salmonella contamination.

Class IIModerate

FDAAug 1, 2019CA, CO, FL +9 more• Milkweed & Monarch, LLC

Ginger Spice Tea (Milkweed & Monarch) – Salmonella Risk (2019)

Salmonella

recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas due to the potential for Salmonella contamination.

Class IIModerate

FDAAug 1, 2019CA, CO, FL +9 more• Milkweed & Monarch, LLC

Entenmann's Little Bites (BIMBO Bakeries) – Plastic Pieces (2019)

Possible presence of small plastic pieces caused by a manufacturing failure.

Class IIModerate

FDAAug 1, 2019AL, AR, CT +34 more• BIMBO Bakeries USA Inc.

BD Vacutainer Collection Set (Becton Dickinson) – Barrel Separation (2019)

Separation of front and rear barrels upon activation of the safety feature that retracts the needle

Low

FDAJul 31, 2019Nationwide• Becton Dickinson & Company

Stryker C2 Nerve Monitor (Stryker) – Usability Issues (2019)

Stryker C2 NerveMonitor's design and instructions may not optimally address usability issues related to the functionality of the device, which may result in use errors potentially causing or contributing to nerve injury.

High

FDAJul 31, 2019Nationwide• Stryker Instruments Div. of Stryker Corporation