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
/
Bea Lydeckers Naturals Inc

Bea Lydeckers Naturals Inc Recalls

All product recalls associated with Bea Lydeckers Naturals 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 3001–3020 of 11124 recalls

Lung & Joint Congestion Supplement (Bea Lydeckers) – Undeclared Soy (2021)

Label declares lecithin but does not declare soy lecithin.

Class IIModerate

FDAJun 21, 2021Nationwide• Bea Lydeckers Naturals Inc

Heart/Blood Vessel Supplement (Bea Lydeckers) – Undeclared Soy (2021)

Label declares lecithin but does not declare soy lecithin.

Class IIModerate

FDAJun 21, 2021Nationwide• Bea Lydeckers Naturals Inc

Nerve & Muscle Plus Supplement (Bea Lydeckers) – Undeclared Soy (2021)

Label declares lecithin but does not declare soy lecithin.

Class II

1...149 150151152 153...557

Page 151 of 557Next

Moderate

FDAJun 21, 2021Nationwide• Bea Lydeckers Naturals Inc

Immune Dietary Supplement (Bea Lydeckers) – Undeclared Soy (2021)

Label declares lecithin but does not declare soy lecithin.

Class IIModerate

FDAJun 21, 2021Nationwide• Bea Lydeckers Naturals Inc

Red Dragon Cheddar Cheese (Somerdale) – Undeclared Wheat (2021)

Cheese label does not declare wheat from ale wash

Class IIModerate

FDAJun 14, 2021MD, MA, NJ +4 more• Wegmans Food Markets, Inc.

Citadel Beds (ArjoHuntleigh) - Power Cord Wear Risk (2021)

Fire/Burn Risk

The IndiGo power cord might wear during use which could lead to its damage, resulting in the cord being cut, burnt or short circuit with limited emission of sparks.

High

FDAJun 10, 2021Nationwide• ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ul. Ks. Piotra Wawrzyniaka 2 Komorniki Poland

Move I 1500 Long Trailer (Karavan) - Improper Spindle Welding (2021)

Karavan Trailers, Inc. (Karavan) is recalling certain 2021 Move I 1500 Long trailers. The wheel spindles were improperly welded to the axle.

High

NHTSAJun 9, 2021Nationwide• KARAVAN

Phytonadione Tablets (AVKARE) – Impurity Concern (2021)

Failed Impurities Specification: Out of specification when measuring the impurity degradant D level.

Class IIILow

FDAJun 9, 2021CA, IN• AVKARE Inc.

RayStation (RaySearch) - Incorrect Beam Positioning (2021)

Initial delivery positions will be set incorrectly when having setup beam(s) at the localization point.

Moderate

FDAJun 8, 2021TN• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

ScanIP Software (Simpleware) - Incorrect Anatomical Orientation (2021)

A issue (bug) has been identified with the interface and image software which could result in anatomical orientation tags/labels being displayed incorrectly. This could result in operator misunderstanding and errors during resampling or re-alignment of image data

Low

FDAJun 4, 2021Nationwide• Simpleware Product Group, SYNOPSYS NORTHERN EUROPE Bradninch Hall Castle Street Exeter United Kingdom

ScanIP Software (Simpleware) - Incorrect Anatomical Orientation (2021)

Low

FDAJun 4, 2021Nationwide• Simpleware Product Group, SYNOPSYS NORTHERN EUROPE Bradninch Hall Castle Street Exeter United Kingdom

Hideout Trailer (Keystone) - LP Gas System Risk (2021)

Fire/Burn Risk

Keystone RV Company (Keystone) is recalling certain 2019 Keystone Bullet, Sprinter, and 2020 Keystone Hideout vehicles equipped with a Winntec model 6020 two-stage propane regulator. The regulator may fail, causing an increase in propane pressure.

High

NHTSAJun 4, 2021Nationwide• KEYSTONE

Spicy Kimchi Aioli (Tulkoff) – Product Recall (2021)

Undeclared Allergen

Tulkoff Food Products Inc., 2229 Van Deman Street, Baltimore MD 21224 has initiated a recall of Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M because of undeclared allergens (Soy, Wheat)

Class IHigh

FDAJun 4, 2021MD, NJ, PA• Tulkoff Food Products, Inc.

Moderna Vaccine Kit (McKesson) - Unsuitable Syringe Risk (2021)

Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.

Moderate

FDAJun 2, 2021Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

RAM 5500 (Stonebrooke) - Brake Caliper Line Issue (2021)

Stonebrooke Equipment INC. (Stonebrooke) is recalling one 2019 RAM 5500 vehicle. The rear brake caliper flexible line can contact suspension components, causing excessive wear and a brake fluid leak.

High

NHTSAJun 2, 2021Nationwide• STONEBROOKE EQUIPMENT

ID.4 (Volkswagen) - Headlight Aim Cap Issue (2021)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 ID.4 vehicles. Caps were installed on the headlight vertical aim instead of the horizontal aim, allowing for horizontal adjustment of the headlight beam. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

High

NHTSAJun 2, 2021Nationwide• VOLKSWAGEN