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R. Walters Limited dba Meninno Brothers Foods

R. Walters Limited dba Meninno Brothers Foods Recalls

All product recalls associated with R. Walters Limited dba Meninno Brothers Foods.

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 1541–1560 of 4465 recalls

Macaroni and Cheese (Hannaford) – Listeria Contamination (2019)

Listeria

Product potentially contaminated with Listeria monocytogenes.

Class IIModerate

FDADec 3, 2019ME, MA, NH +1 more• R. Walters Limited dba Meninno Brothers Foods

Degania Silicone, Ltd. Degania Bet Dganya Bet Israel: Medline Thermistor Foley Catheter 14 FR 5-10 ml, non ster...

Temperature deviation did not meet release specifications

FDADec 2, 2019IL• Degania Silicone, Ltd. Degania Bet Dganya Bet Israel

Stryker GmbH Bohnackerweg 1 Selzach Switzerland: Stryker Pin To Rod Coupling External Fixation System Hof...

Pin To Rod Coupling could not clamp the pin and rod as intended

1...76 777879 80...224

Page 78 of 224Next

FDA

Nov 21, 2019

Nationwide

• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

B. Braun Medical, Inc.: Outlook Safety Infusion System Y-type Blood Set, Catalog ...

Potential for leakage at the joint between the blood filters and tubing

FDANov 20, 2019Nationwide• B. Braun Medical, Inc.

Airome Essential Oils (B&B Acquisition) – packaging risk (2019)

This recall involves Airome Wintergreen 100% pure essential oils in 0.5- and 0.34-fluid-ounce amber glass dropper bottles sold without a child-resistant cap. It also includes Airome Deep Soothe 100% pure essential oils in 0.5-fluid-ounce amber glass dropper bottles sold without a child-resistant cap. Each bottle has a black cap and blue label with either "Airome Wintergreen 100% Pure Essential Oil Stimulate" or "Airome Deep Soothe 100% Pure Essential Oil Cool" printed on the front. A UPC code unique to each type of recalled bottle -83324503131, 833245034567, or 833245035977 - is printed on the bottom of the gift box in which the bottles were sold. The Arome Wintergreen 100% Pure Essential Oil Stimulate was sold separately and as part of a 3-pack "Focus & Concentrate Essential Oil Gift Set."

CPSCNov 20, 2019Nationwide• B&B Acquisition, of Salt Lake City, Utah

B. Braun Medical, Inc.: Y-Type Blood Set, Catalog Number 490293

Potential for leakage at the joint between the blood filters and tubing

FDANov 20, 2019Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Safeline Y-Type Blood Set, Catalog Number NF5140

Potential for leakage at the joint between the blood filters and tubing

FDANov 20, 2019Nationwide• B. Braun Medical, Inc.

2020 THOMAS BUILT BUSES SAF-T-LINER HDX Recall: POWER TRAIN:AUTOMATIC TRANSMISSION:TORQUE CONVERTER

Daimler Trucks North America LLC (DTNA) is recalling certain 2018-2020 Thomas Built Saf-T-Liner HDX school buses equipped with Detroit DD8 Engines and Allison Transmissions. The Flex-Plate/Torque Converter fasteners may have been insufficiently tightened.

NHTSANov 19, 2019Nationwide• THOMAS BUILT BUSES

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation stand-alone software treatment planning system...

Editing a static arc beam may unexpectedly set the MU of the beam to its initial default value of 200 MU. If the bug is triggered, the dose is invalidated and needs to be recalculated before the plan can be approved or exported.

FDANov 18, 2019Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Nucletron BV Waardgelder 1 POBox 930 Veenendaal Netherlands: There is a complaint regarding internal check cable guide...

A component failure may lead to treatment interruption or incorrect source positioning.

FDANov 18, 2019Nationwide• Nucletron BV Waardgelder 1 POBox 930 Veenendaal Netherlands

Abbott Diabetes Care, Inc.: Optium EZ Blood Glucose Monitoring System, UDI: 000938157...

Instructions sent in a letter or in instructions for use for disinfecting blood glucose and/or ketone meters were distributed but not cleared by the U.S. FDA, and devices were not cleared for multiple-patient use. Instructions could lead to inappropriate meter disinfection or improper handling of contaminated meters, which may cause infection or exacerbation of an existing infection.

FDANov 14, 2019AL, CA, CT +29 more• Abbott Diabetes Care, Inc.

Abbott Diabetes Care, Inc.: Precision Xtra Blood Glucose & Ketone Monitoring System, ...

FDANov 14, 2019AL, CA, CT +29 more• Abbott Diabetes Care, Inc.

Abbott Diabetes Care, Inc.: FreeStyle Precision H Blood Glucose and Ketone Monitoring...

FDANov 14, 2019AL, CA, CT +29 more• Abbott Diabetes Care, Inc.

Abbott Medical: CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compa...

A manufacturing error caused a single lot of 10mm active tip length Cannulas to be labeled as 5mm active tip length cannulas.

FDANov 11, 2019Nationwide• Abbott Medical

Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany: ARCHITECT HAVAB-G Calibrator, REF 6L27-01

Abbott has identified that Calibrator lot 08219BE00 is potentially impacted by an increase in Relative Light Units (RLUs) up to 94%. It has been confirmed that the increase in the calibrator RLU values may cause a decrease in the control values and patient results. Patient values generated using the impacted calibrator lot 08219BE00 may have changed interpretation from reactive to falsely non reactive. Results impacted may present as a (falsely) non reactive result that fall in the range between 0.50 to 0.99 S/CO.

FDANov 7, 2019AZ, CA, CO +20 more• Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany

2019 BLUE BIRD VISION Recall: EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH

Blue Bird Body Company (Blue Bird) is recalling certain 2013-2020 Vision transit buses equipped with Ford engines. The brake light switch mounting bracket may have caused the brake light switch to be incorrectly adjusted at installation and/or the brake light switch mounting bracket may deform when the driver allows the brake pedal to return forcibly. An incorrectly adjusted brake light switch or deformed brake light switch mounting bracket may cause the brake lights to illuminate continuously.

NHTSANov 6, 2019Nationwide• BLUE BIRD

2014 BLUE BIRD VISION Recall: EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH

Blue Bird Body Company (Blue Bird) is recalling certain 2013-2020 Vision school buses equipped with Ford engines. The brake light switch mounting bracket may have caused the brake light switch to be incorrectly adjusted at installation and/or the brake light switch mounting bracket may deform when the driver allows the brake pedal to return forcibly. An incorrectly adjusted brake light switch or deformed brake light switch mounting bracket may cause the brake lights to illuminate continuously.

NHTSANov 6, 2019Nationwide• BLUE BIRD

King Systems Corp. dba Ambu, Inc.: King Vision Video Adapter Size 1/2. Laryngoscope used to...

Exhibiting a reversed image. Although the image may appear normal, the users actions will be reversed on the display for left and right directions.

FDANov 5, 2019Nationwide• King Systems Corp. dba Ambu, Inc.

Nut Bread (Beatrice Bakery) – Mold Growth (2019)

Nut bread show growth of mold before their best by dates

Class IIModerate

FDANov 5, 2019AR, IN, NJ +2 more• Beatrice Bakery Co

Bio-Rad Laboratories, Inc.: BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incomp...

A new lot of ANA screen control and any subsequent control lots are incompatible with older lot numbers of ANA calibrators and ANA reagent packs.

FDANov 1, 2019Nationwide• Bio-Rad Laboratories, Inc.