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Panaderia Guatemex

Panaderia Guatemex Recalls

All product recalls associated with Panaderia Guatemex.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 2141–2160 of 25000 recalls

Curenitos (Panaderia Guatemex) – Undeclared Soy (2024)

Undeclared Allergen

Undeclared Allergen - Soy

Class IIModerate

FDAJul 2, 2024GA, KY, TN• Panaderia Guatemex

Casco (Panaderia Guatemex) – Undeclared Soy (2024)

Undeclared Allergen

Undeclared Allergen - Soy

Class IIModerate

FDAJul 2, 2024GA, KY, TN• Panaderia Guatemex

Sheca Redonda (Panaderia Guatemex) – Undeclared Soy (2024)

Undeclared Allergen

Undeclared Allergen - Soy

1...106 107108109 110...1250

Page 108 of 1250Next

Moderate

FDAJul 2, 2024GA, KY, TN• Panaderia Guatemex

Cortado Rojo (Panaderia Guatemex) – Undeclared Soy (2024)

Undeclared Allergen

Undeclared Allergen - Soy

Class IIModerate

FDAJul 2, 2024GA, KY, TN• Panaderia Guatemex

Champurradas (Panaderia Guatemex) – Undeclared Soy (2024)

Undeclared Allergen

Undeclared Allergen - Soy

Class IIModerate

FDAJul 2, 2024GA, KY, TN• Panaderia Guatemex

Pegado (Panaderia Guatemex) – Undeclared Soy (2024)

Undeclared Allergen

Undeclared Allergen - Soy

Class IIModerate

FDAJul 2, 2024GA, KY, TN• Panaderia Guatemex

BioPince Biopsy Instrument (Argon Medical) – Packaging Breach (2024)

Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of micro-organisms into the access site, which could lead to an infectious process, bacteremia, or sepsis.

FDAJul 2, 2024Nationwide• Argon Medical Devices, Inc

Everest Bipolar Cutting Forceps (Olympus) – Packaging Breach (2024)

Fractures and breakages in packaging trays and Tyvek covers, which may result in a sterility breach

FDAJul 1, 2024Nationwide• Olympus Corporation of the Americas

2025 Coachmen Cross Trail (Coachmen) – Ladder Installation Problem (2024)

Forest River, Inc. (Forest River) is recalling certain 2024-2025 Cross Trail motorhomes. The ladder receiver may have been incorrectly installed without the backer, which can cause the ladder to detach.

NHTSAJun 28, 2024Nationwide• COACHMEN

Fludrocortisone Acetate Tablets (Teva) – Impurity Concerns (2024)

Failed Impurities/Degradation Specifications: Product is being recalled due to API related substances and unknown impurities that are above the specification limits.

Class IIModerate

FDAJun 28, 2024Nationwide• Teva Pharmaceuticals USA, Inc

2025 Coachmen Cross Trail (Coachmen) – Ladder Receiver Issue (2024)

Forest River, Inc. (Forest River) is recalling certain 2024-2025 Cross Trail motorhomes. The backer on the ladder receiver may not have been installed, which can cause the ladder to detach.

NHTSAJun 28, 2024Nationwide• COACHMEN

Pravastatin Sodium Tablets (Glenmark) – Dissolution Failure (2024)

Failed Dissolution Specifications: results below specifications

Class IIModerate

FDAJun 28, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

IntelliVue Patient Monitor MX400 (Philips) – Software Configuration (2024)

Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded with Incorrect Software Options. Changes were made to reflect some options becoming standard capabilities for software-version N.x. In the process, the entitlements of software options MOS, M06, and M20 were removed for software versions L.x and M.x. As a result of these changes Patient Monitors manufactured with or updated to the latest versions of software L.x or M.x will not offer the capabilities> Mmonitors with software version K.x may experience this issue too, due to software version K being out of support and the devices being provided with L.x entitlements offered by software options MOS, M06, and M20. Potential for incorrect or delayed treatment for the patient,

FDAJun 28, 2024Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX500 (Philips) – Software Configuration (2024)

Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded with Incorrect Software Options. Changes were made to reflect some options becoming standard capabilities for software-version N.x. In the process, the entitlements of software options MOS, M06, and M20 were removed for software versions L.x and M.x. As a result of these changes Patient Monitors manufactured with or updated to the latest versions of software L.x or M.x will not offer the capabilities> Mmonitors with software version K.x may experience this issue too, due to software version K being out of support and the devices being provided with L.x entitlements offered by software options MOS, M06, and M20. Potential for incorrect or delayed treatment for the patient,

FDAJun 28, 2024Nationwide• Philips North America Llc

Daikin FIT Heat Pumps (Daikin) – potential equipment failure (2024)

This recall involves Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps that provide heating and cooling. The recalled units are beige and the model name is printed on the outside of the unit. The model number is located on the serial plate on the side of the unit. The following model numbers are included in this recall: Recalled Daikin FIT Recalled Amana S-Series Recalled Goodman SD DZ6VSA1810-AA ASZS601810-AA GSZS601810-AB DZ6VSA1810-AB ASZS601810-AB GSZS602410-AB DZ6VSA2410-AA ASZS602410-AA GSZS603010-AB DZ6VSA2410-AB ASZS602410-AB GSZS603610-AB DZ6VSA241E-AB ASZS60241E-AB DZ6VSA3010-AA ASZS603010-AA DZ6VSA3010-AB ASZS603010-AB DZ6VSA3610-AA ASZS603610-AA DZ6VSA3610-AB ASZS603610-AB

CPSCJun 27, 2024Nationwide• Daikin Comfort Technologies Manufacturing L.P., of Houston, Texas

Co-op Cycles REV Bicycles (REI) – fall injury hazard (2024)

This recall involves REI Co-op Cycles REV 12-, 16-, or 20-inch kid's bicycles (all model years 2022-2024). Serial numbers included in the recall begin with "ET22," "ET23," "01VX" or "07VX." The serial number is printed underneath the bike frame on the bottom bracket or down tube. Brand Model SKU/Article # Color Co-op Cycles REV 12 Kids Bike 190741 BONDI (green) Co-op Cycles REV 12 Kids Bike 190741 PENCIL (yellow) Co-op Cycles REV 16 Kids Bike 190742 SURFS UP (blue) Co-op Cycles REV 16 Kids Bike 190742 CATCH UP (red) Co-op Cycles REV 16 Kids Bike 190743 FOUR LEAF (green) Co-op Cycles REV 20 Kids Bike 190743 PLUM BURST (purple)

CPSCJun 27, 2024Nationwide• RECREATIONAL EQUIPMENT INC. (REI), of Sumner, Washington

Premo Turkey & Swiss (Lipari Foods) – Salmonella Contamination (2024)

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Cyanocobalamin Injection (Zydus) – Glass Particulate Risk (2024)

Presence of particulate matter: glass

Class IIModerate

FDAJun 27, 2024TN• Zydus Pharmaceuticals (USA) Inc

Premo King Club Footlong (Lipari Foods) – Salmonella Contamination (2024)

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Premo Meat Lovers (Lipari Foods) – Salmonella Contamination (2024)

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.