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NRS Enterprises, Inc. dba Sunflour Bakery

NRS Enterprises, Inc. dba Sunflour Bakery Recalls

All product recalls associated with NRS Enterprises, Inc. dba Sunflour Bakery.

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Recall Summary

Total Recalls

1000

Past Year

442

Class I (Serious)

138

Most Recent

Dec 2025

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 801–820 of 7663 recalls

Poppy Coffee Cake (Sunflour Bakery) – Undeclared Yellow #5 (2024)

Undeclared Allergen

Undeclared Yellow #5

Class IIModerate

FDAMar 8, 2024CA• NRS Enterprises, Inc. dba Sunflour Bakery

Marzipan Coffee Cake (Sunflour Bakery) – Undeclared Yellow #5 (2024)

Undeclared Allergen

Undeclared Yellow #5

Class IIModerate

FDAMar 8, 2024CA• NRS Enterprises, Inc. dba Sunflour Bakery

Eco Terra Hybrid Mattress (Sleep Technologies) – Fire Hazard (2024)

Fire/Burn Risk

This recall involves model ECO TERRA Eco Terra Mattresses manufactured from Aug 5, 2022 to Aug 18, 2022. The mattresses are 10 inches thick with a top panel that is ivory and quilted. The side panel is brown knit quilted with horizontal lines, and the top and bottom tape edges are ivory. The manufacture dates and model name "ECO TERRA" are located on the mattress label, sewn into the cover.

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High

CPSCMar 7, 2024Nationwide• Sleep Technologies Inc., d/b/a The Natural Latex Co. of Camarillo, California

KWIK-STIK Rhizopus Stolonifer (Microbiologics) – Fungal Contamination (2024)

The positive control material (Rhizopus stolonifer) within the KWIK-STIK assembly was contaminated with another fungal organism (Aspergillus brasiliensis). As a result, users may observe A. brasiliensis growth when using the control material.

Moderate

FDAMar 6, 2024Nationwide• Microbiologics Inc

Ground Cinnamon (Colonna Brothers) – Lead Levels (2024)

Elevated lead levels in cinnamon

Class IIModerate

FDAMar 6, 2024Nationwide• Colonna Brothers Inc.

Alinity i Anti-HCV Reagent Kit (Abbott) – False Elevated Results (2024)

Customer complaints were received regarding falsely elevated results for some patient samples. Internal studies with customer return samples confirmed potential interactions that may lead to falsely elevated results when processed as below on the same instrument: " ARCHITECT Syphilis TP (LN 8D06) and/or ARCHITECT AdviseDx SARS-CoV-2-IgG II (LN 6S60) precedes ARCHITECT Anti-HCV testing (LN 1L79). " Alinity i Syphilis TP (LN 07P60) precedes Alinity i Anti-HCV testing (LN 08P05).

Low

FDAMar 4, 2024Nationwide• Abbott GmbH Max-Planck-Ring 2 Wiesbaden Germany

ARCHITECT Anti-HCV Reagent Kit (Abbott) – False Elevated Results (2024)

Low

FDAMar 4, 2024Nationwide• Abbott GmbH Max-Planck-Ring 2 Wiesbaden Germany

Mercedes-Benz G 550 (Mercedes-Benz) – A/C System Filling Issue (2024)

Fire/Burn Risk

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2022-2023 AMG G 63 and 2023 G 550 vehicles. The air-conditioning system may not have been filled with the correct refrigerant.

High

NHTSAMar 1, 2024Nationwide• MERCEDES-BENZ

Mercedes-Benz Sprinter 4500 (Mercedes-Benz) – Wiring Harness Chafe (2024)

Fire/Burn Risk

Daimler Vans USA, LLC (DVUSA) is recalling certain 2023 Mercedes-Benz Sprinter vehicles. The main wiring harness may chafe against the drive shaft and short circuit, which can result in a loss of drive power, power steering, and brake system control.

High

NHTSAMar 1, 2024Nationwide• MERCEDES-BENZ

Thyroid Full Strength (Specialty Labs) – stability failure (2024)

Failed Stability Specifications

Class IIModerate

FDAMar 1, 2024Nationwide• Specialty Process Labs LLC

Thyroid USP (Specialty Labs) – stability failure (2024)

Failed Stability Specifications

Class IIModerate

FDAMar 1, 2024Nationwide• Specialty Process Labs LLC

Phenylephrine HCl (SSM Health) – sterility validation (2024)

Lack of Assurance of Sterility: Firm did not perform process validation.

Class IIModerate

FDAFeb 29, 2024MO• SSM Health Care St. Louis DBA SSM St. Clare Health Center

FentaNYL Citrate (SSM Health) – sterility validation (2024)

Lack of Assurance of Sterility: Firm did not perform process validation.

Class IIModerate

FDAFeb 29, 2024MO• SSM Health Care St. Louis DBA SSM St. Clare Health Center

MERCEDES-BENZ TOURRIDER BUSINESS (MERCEDES-BENZ) – Roof Exit Issue (2024)

Daimler Coaches North America (Daimler Coaches) is recalling certain 2022-2024 Mercedes Benz Tourrider Business and Tourrider Premium vehicles. The roof hatch handle may break. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 217, "Bus Emergency Exits and Window Retention and Release."

High

NHTSAFeb 26, 2024Nationwide• MERCEDES-BENZ

Altair Patient Lift (Human Care) – Hanger Bar Risk (2024)

Patient lift hanger bar may come loose, which could potentially pose risks to patients.

High

FDAFeb 23, 2024Nationwide• Human Care Hc Sweden Ab Arstaangsvagen 21 B Stockholm Sweden

RayStation Software (RaySearch) – Material Override Error (2024)

A use error that has occurred with RayStation/RayPlan, where material override using Silicon, Si, was incorrectly selected for a silicone gel polymer implant.

High

FDAFeb 23, 2024Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

MERCEDES-BENZ TOURRIDER BUSINESS (MERCEDES-BENZ) – Mobility Equipment (2024)

Daimler Coaches North America (Daimler Coaches) is recalling certain 2022-2024 Mercedes Benz Tourrider Business and Mercedes Benz Tourrider Premium vehicles equipped with BraunAbility wheelchair lifts. The outer barrier may deploy unexpectedly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 403, "Platform Lift Systems."

High

NHTSAFeb 23, 2024Nationwide• MERCEDES-BENZ

Raiz de Tejocote Supplements (Backstage Center) - toxic ingredient (2024)

The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.

Class IHigh

FDAFeb 23, 2024Nationwide• Backstage Center DBA CTC Seller

3M Tube Securement Device (3M) – Manufacturing Defect (2024)

Manufacturing nonconformities are in some lots of the Tube Securement Device, such as the top film layer may be partially or completely missing and some devices may exhibit the appearance of an incorrect shape due to excess material not being removed from the product liner.

Moderate

FDAFeb 20, 2024Nationwide• 3M Company Health Care Business 3m Center

Moxifloxacin Single-Dose Vial (Denver Solutions) – glass delamination (2024)

Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.

Class IIModerate

FDAFeb 20, 2024Nationwide• Denver Solutions, LLC DBA Leiters Health