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B&W TRAILER HITCHES

B&W TRAILER HITCHES Recalls

All product recalls associated with B&W TRAILER HITCHES.

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Recall Summary

Total Recalls

1000

Past Year

169

Class I (Serious)

125

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 481–500 of 1553 recalls

B&W TRAILER HITCHES LOCKING RECEIVER HITCH PI Equipment Recall: TRAILER HITCHES

B&W Custom Truck Beds, Inc. (B&W) is recalling certain 5/8" Stainless Steel Locking Receiver Hitch Pins, part number TS51237 and TS51237JD. A defective hitch pin lock can be removed without a key, allowing the ball mount to detach from the receiver tube.

NHTSAMay 5, 2021Nationwide• B&W TRAILER HITCHES

Almond Butter (Natural Way) – Undeclared Peanuts (2021)

Undeclared Nuts

Potential to contain undeclared peanuts

Class IHigh

FDAMay 4, 2021Nationwide• Simkins Brothers Sweets, LLC dba Natural Way Food Group

2021 BMW M340I Recall: SEAT BELTS:FRONT:BUCKLE ASSEMBLY

BMW of North America, LLC (BMW) is recalling certain 2021 330i, 330i xDrive, M340i, M3, and 330e xDrive vehicles. The bolt securing the seat belt assembly to the frame was not tightened to specification.

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NHTSAApr 28, 2021Nationwide• BMW

Uplift Blood Orange Kombucha (Brew Dr) – yeast contamination (2021)

Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.

Class IIModerate

FDAApr 26, 2021Nationwide• BREW DR KOMBUCHA LLC

Uplift Mango Passionfruit Kombucha (Brew Dr) – yeast contamination (2021)

Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.

Class IIModerate

FDAApr 26, 2021Nationwide• BREW DR KOMBUCHA LLC

Uplift Blueberry Raspberry Kombucha (Brew Dr) – yeast contamination (2021)

Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.

Class IIModerate

FDAApr 26, 2021Nationwide• BREW DR KOMBUCHA LLC

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation (Treatment Planning System) Model Number RaySt...

Evaluation of a clinical goal for the voxelwise worst dose distributions may be misleading after editing the clinical goal. It also describes an issue with contouring when the spacing between slices is d 1 mm, present in RayStation/RayPlan versions from 6 up to 10A.

FDAApr 21, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation standalone software radiation therapy treatmen...

When using more than one plan in a treatment course, the Total dose display in Dose tracking may be incorrect. There may be a mismatch between the fractions that appear as selected in the Treatment course list in Dose tracking and the fractions that are included in the dose summation. The issue only affects RayTreat users and only the Total dose option. Accumulation and other options in Dose tracking are correct.

FDAApr 7, 2021TN• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation Model Number: (9A)9.0.0.113, 9B (9.1.0.933), 9...

Flags edited in RayCare after a patient has been checked in may not always be updated in RayTreat.

FDAMar 25, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

2021 BMW X3 Recall: FUEL SYSTEM, GASOLINE:STORAGE:TANK ASSEMBLY

Fire/Burn Risk

BMW of North America, LLC (BMW) is recalling certain 2021 X3 sDrive30i, X3 xDrive30i, X3 M40i, X3M, and X4, and 2021 X4 xDrive30i vehicles. The inlet check valve weld may fail, allowing the filling pipe to separate from the fuel tank.

NHTSAMar 24, 2021Nationwide• BMW

YTL Log Splitters (Briggs & Stratton) – Injury Hazard (2021)

The recall involves YTL log splitters powered by Briggs & Stratton 250cc engine, with engine model number 15T232-0011-F8 and serial numbers 1904085275251 through 1905085786452; 1906146333235 through 2004080670911; and 1912319442579 through 2012073736714. The engine's model number is printed on the valve cover and the engine's serial number is printed on the blower housing cover. The log splitters are sold under the following brands: Black Diamond (model number BDBS32T - 32 ton); Crimson (model number YTL-590-012 - 32 ton); Lumberjack (model number YTL-007-414); Performance Built (model number YTL-007-308); and Brute (model numbers YTL-140-701 -30 ton and YTL-140-743 - 35 ton).

CPSCMar 18, 2021Nationwide• Briggs & Stratton, of Wauwatosa, Wis. (engine)

2021 BMW M440I Recall: AIR BAGS:SIDE/WINDOW:HEAD

BMW of North America, LLC (BMW) is recalling certain 2021 430i and M440i 4 Series Convertible vehicles. In certain side-impact crashes, the head-thorax air bag may not deploy as intended.

NHTSAMar 15, 2021Nationwide• BMW

6-Foot Seminar Tables (Lifetime) – injury risk (2021)

This recall involves Lifetime Products 6-Foot Seminar Tables with model #80176. The tables have gray metal frames and white plastic tops. The tables measure 6 feet long by 18 inches wide by 28 inches high. The "Lifetime" logo is molded into each end of the upper surface of the table top. A green product ID sticker located on the underside of the table has the model number and the year and chronological day of manufacture in the first five digits (Example: June 23, 2020 = 20175), followed by a two-digit number for the factory. The recalled tables were manufactured between August 7, 2016 (16220) and June 23, 2020 (20175).

CPSCMar 10, 2021Nationwide• Kingtec Group Vietnam Co. LTD, of Ben Cat Town, of Binh Duong Province, Vietnam

2021 BMW X7 Recall: SEATS:MID/REAR ASSEMBLY:HEAD RESTRAINT

BMW of North America, LLC (BMW) is recalling certain 2021 X5 sDrive40i, X5 xDrive50i, X5 M50i, X5 xDrive45e, 2021 X7 xDrive40i, X7 M50i, and XB7 vehicles. The head restraints on the second-row outer seats may be the incorrect type for the vehicle.

NHTSAMar 10, 2021Nationwide• BMW

2016 CUSTOM TRUCK & BODY WORKS FORD F-550 Recall: EXTERIOR LIGHTING

Custom Truck And Body Works (Custom Truck) is recalling one 2016 Ford F550 vehicle and one 2018 International 4000 vehicle equipped with 7x9 combination LED Stop-Tail-Turn reverse lights. The lights may be too bright, exceeding the maximum light output allowed which may adversely affect the vision of drivers. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment."

NHTSAMar 5, 2021Nationwide• CUSTOM TRUCK & BODY WORKS

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayCare 3B (3.1.0.60341) - Product Usage: Intended Use On...

Patient related messages created in RayCare 3B, RayCare 4A will be lost when upgrading from RayCare 2 to RayCare 3B or later

FDAMar 3, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Sweet Heat Pepper Dip (B&G) – Undeclared milk (2021)

Cream Cheese and Sour Cream are declared, but milk is not declared on label.

Class IIModerate

FDAFeb 27, 2021ID, IN, WA• B&G Sweet Heat Peppers

Biosense Webster, Inc.: Biosense Webster, CARTO VIZIGO, Bi-Directional Guiding Sh...

There is a potential for the hemostatic valve to dislodge while introducing the dilator or device into the sheath. This could result in minor bleeding and/or embolism

FDAFeb 26, 2021Nationwide• Biosense Webster, Inc.

Essential Oils (deSensua) – Safety Failure (2021)

This recall involves 1/2 fl. oz (15 mL) amber glass bottles with black caps of deSensua Wintergreen Essential Oil, Birch Essential Oil and Pain Soother Essential Oil. The black, gold and blue labels on each bottle displays the deSensua logo, product name and the volume amount of the bottle. The Wintergreen Essential Oil has UPC code 760921403266, the Birch Essential Oil has UPC code 760921403129 and the Pain Soother Essential Oil has UPC code 760921403051 printed on the back of the label.

CPSCFeb 25, 2021Nationwide• MTIG Productions LLC, dba deSensua, of Buffalo, Wyo.

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation 4.5, 4.7, 4.9, 5, 6, 7, 8A, 8B, 9A, 9B, 10A, 1...

For some LINAC types, merging clinical beams with beams of approximate dose may lead to the approximate dose erroneously labeled as clinical dose. Merge beams can be used manually, in scripting, or as part of the Automated breast planning feature. In some cases, when merging two beams where the first beam has clinical dose and the second beam has approximate dose, the dose of the resulting beam will be labeled as Clinical, although dose for some of the beam segments is still calculated with the SVD dose engine and it should be labeled Approximate: Mixed dose. The difference between approximate and final Clinical dose is in most cases small, but there can be body sites such as lung where the difference can be significant.

FDAFeb 22, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden