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
/
NATURE'S SUNSHINE PRODUCTS

NATURE'S SUNSHINE PRODUCTS Recalls

All product recalls associated with NATURE'S SUNSHINE PRODUCTS.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

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 1521–1540 of 4099 recalls

Love & Peas Meal Replacement (Nature's Sunshine) - Potential Milk Trace (2021)

The firm was notified by an ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.

Class IHigh

FDAApr 12, 2021Nationwide• NATURE'S SUNSHINE PRODUCTS

SPINEART SA Chemin Du Pre-Fleuri 3 Plan-Les-Ouates Switzerland: PERLA TL Lateral Connector Open - Product Usage: intended...

Due to external labelling error/mix-up. Affected product external labels list the incorrect rod size.

FDAApr 9, 2021Nationwide• SPINEART SA Chemin Du Pre-Fleuri 3 Plan-Les-Ouates Switzerland

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.

1...75 767778 79...205

Page 77 of 205Next

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

Deep Blue Essential Oils (doTERRA) – Safety Concerns (2021)

This recall involves doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils in 10 mL glass bottles with rollerball applicator and black cap. The product name, volume amount, SKU, and doTERRA logo are printed on the product labels. The following lot number can be found on the bottom of the bottle: Name Size Lot Number SKU Deep Blue 10 ml 183055, 183232, 190882, 191362, 191484, 192563, 192694, 200853, 202203, 202412, 201622, 202262 60200144 PastTense 10 ml 182621, 190072, 190452, 190512, 190573, 190642, 190662, 190702, 190801, 190921, 191232, 191404, 193451, 200242, 200422, 200932, 201292, 201351, 201392, 201401, 201471, 201481, 201493, 201541, 201551, 201571, 201603, 201673, 201744, 201754, 201822, 201971, 202043 31350001 Deep Blue Touch 10 ml 183094, 190802, 192314, 192666, 193222, 201141, 201923 60200145

CPSCApr 1, 2021Nationwide• doTERRA International LLC, of Pleasant Grove, Utah

Omnia SRL Via Fratelli Cairoli 5 Fidenza Italy: Omnia Soft Tissue Punch is a dental instrument designed t...

Omnia SRL received a notification from the contract manufacturer informing them of inadequate sterilization processes which have been taking place at their contracted sterilizing facility since 2016.

FDAMar 30, 2021AK, CA, IL +5 more• Omnia SRL Via Fratelli Cairoli 5 Fidenza Italy

Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland: Calibration Serum Level 3 (CAL 3) - multi-analyte mixture...

Randox can confirm a positive bias for Total Bilirubin and Direct Bilirubin of up to +15% across the assay ranges when using calibrator CAL2351, lot 1162UE. The positive bias has been attributed to bilirubin instability in the calibrator and is evident in both Quality Control (QC) and Patient samples.

FDAMar 29, 2021CA, CT, IL +13 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Atos Medical AB Kraftgatan: Provox Life Night HME, Catalogue Number 8262 - Product Us...

Provox Life Night HME may be incorrectly inserted sideways or forcefully through the adhesive coupling potentially occluding or blocking the stoma.

FDAMar 29, 2021Nationwide• Atos Medical AB Kraftgatan

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

Whole Foods Market Cooked Shrimp (Avanti) – Packaging Error (2021)

One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.

Class IIILow

FDAMar 20, 2021Nationwide• Avanti Frozen Foods Private Limited

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)

Sp-4 Solution (Washington Homeopathic) – Ingredient Error (2021)

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

Class IIILow

FDAMar 18, 2021CO, MD, TX• Washington Homeopathic Products, Inc.

LCL-2-0191 (Washington Homeopathic) – Ingredient Error (2021)

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

Class IIILow

FDAMar 18, 2021CO, MD, TX• Washington Homeopathic Products, Inc.

Macula Pellets (Washington Homeopathic) – Ingredient Error (2021)

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

Class IIILow

FDAMar 18, 2021CO, MD, TX• Washington Homeopathic Products, Inc.

Revive Three Wick Soy Candles (EAP) – fire hazard (2021)

Fire/Burn Risk

This recall involves the Revive Three Wick Soy Candles in Winter Cedar and Warm Spiced Latte scents. The candles come in glass containers with metal lids. "Revive" and the scent type are printed on a label on the front of the container. SKU 1010030041 (for the winter cedar-scented candle) or 1010030040 (for the warm spiced latte-scented candle) is printed on the purchase receipt.

CPSCMar 11, 2021Nationwide• EAP Innovations, of Mt. Pleasant, Pa.

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

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

Acetaminophen Tablets (A-S Medication) – labeling mixup (2021)

Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen 500mg Extra Strength, 100 count, included in Health Essential Kits, labeled incorrectly with a prescription drug label instead of an OTC drug label.

Class IHigh

FDAMar 2, 2021Nationwide• A-S Medication Solutions LLC.

Imatinib Mesylate Tablets (Dr. Reddy's) – Poisoning Risk (2021)

This recall involves blister packages of prescription medications. The name and strength of the medication, "For Institutional Use only," "Rx Only," lot number and expiration date are printed on the outside of the package as well as on the individual blister units. The Dr. Reddy's logo and NDC number are printed on the outside of the package. The recalled medications include the following: Recalled Prescription Drugs NDC Numbers Carton Configurations Lot Numbers Expiration Dates Imatinib Mesylate Tablets 100 mg 43598-344-31 3 blister cards of 10 tablets H2000138 2022-0630 Imatinib Mesylate Tablets 400 mg 43598-345-31 3 blister cards of 10 tablets H2000127 2022-0630 Pregabalin Capsules 50 mg 43598-292-66 5 blister cards of 10 capsules T900876 2021-0630 Pregabalin Capsules 75 mg 43598-293-66 5 blister cards of 10 capsules T901021 2021-0731 Pregabalin Capsules 100 mg 43598-294-66 5 blister cards of 10 capsules T901022 2021-0731 Pregabalin Capsules 150 mg 43598-295-66 5 blister cards of 10 capsules T901023 2021-0731 Sevelamer Carbonate Tablets 800 mg 55111-789-11 4 blister cards of 25 tablets T801003, T000009, T900221 2020-1031, 2021-1231, 2021-0228 Tadalafil Tablets 5 mg 43598-575-31 3 blister cards of 10 tablets T000376 2022-0131 Tadalafil Tablets 20 mg 43598-573-31 3 blister cards of 10 tablets T000425 2022-0228

CPSCFeb 25, 2021Nationwide• Dr. Reddy's Laboratories, Ltd., of India

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

Somatex Medical Technologies GMBH Hohenzollerndamm 150-151 Berlin Germany: Thread-like wire marker

This recall has been initiated due to the risk of wire splintering after contact with a cautery device during the removal of a lesion. There is a potential risk that wire fragments are not removed during the procedure and stays inside the patient's body.

FDAFeb 3, 2021MO, NJ, OH• Somatex Medical Technologies GMBH Hohenzollerndamm 150-151 Berlin Germany