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Washington Homeopathic Products, Inc.

Washington Homeopathic Products, Inc. Recalls

All product recalls associated with Washington Homeopathic Products, Inc..

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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 1721–1740 of 4099 recalls

Natrum Phosphoricum 6X Tablets (Washington Homeopathic) – Manufacturing Deviation (2019)

CGMP Deviations: products were not manufactured under current good manufacturing practices.

Class IIModerate

FDANov 8, 2019Nationwide• Washington Homeopathic Products, Inc.

Silicea Tablets (Washington Homeopathic) – Manufacturing Practices (2019)

CGMP Deviations: products were not manufactured under current good manufacturing practices.

Class IIModerate

FDANov 8, 2019Nationwide• Washington Homeopathic Products, Inc.

Pip Pop Movie Theater Popcorn (Water Gardens) – Foreign Material (2019)

Foreign material determined to be part of packaging was found in 24 oz. bags of Pip Pop Movie Theater Popcorn produced on multiple dates.

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Class IIModerate

FDANov 7, 2019CO, ID, IN +4 more• Water Gardens Confections LLC

2015 MCELRATH TRAILERS VX Recall: EXTERIOR LIGHTING

Conel, LLC dba McElrath Trailers (McElrath Trailers) is recalling certain 2014-2019 VX trailers. The side marker LED lights may be missing reflex reflectors. 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."

NHTSANov 5, 2019Nationwide• MCELRATH TRAILERS

Blackhawk T-Series Gun Holsters (Federal Cartridge) – Injury Risk (2019)

Fire/Burn Risk

This recall involves the Blackhawk T-Series black gun holster L2C made of molded plastic material. The black holster is designed to be used with Sig Sauer P320/P250 civilian firearms that clip onto the user's belt. "2101213 A" is printed on the outside of the recalled gun holsters.

CPSCOct 22, 2019Nationwide• Federal Cartridge Company, of Manhattan, Mont. d/b/a Blackhawk, Virginia Beach, Va.

PF-Succinylcholine Chloride (Nephron) – Incorrect Labeling (2019)

Incorrect labeling: Incorrect or missing lot and/or exp date

Class IIILow

FDAOct 21, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Cuattro LLC: CuattroDR System Software, REF: SWR-00069-MD, UDI: B269SW...

There is a potential that an image from a previous patient study to show up in a later patient study. This may result in misdiagnosis of the correct patient.

FDAOct 15, 2019AR, MI, NJ +2 more• Cuattro LLC

Natural Grocers Organic Soybeans (Natural Grocers) – mold potential (2019)

Firm is recalling two lots of 2 lb. organic soybeans because they have the potential to contain mold.

Class IIILow

FDAOct 14, 2019Nationwide• Vitamin Cottage Natural Foods Market, Inc DBA Natural Grocers

Signature Orthopaedics Europe Ltd Unit A, IDA Business & Technology Park Garrycastle Athlone Ireland: Encina HA Femoral Stem, Size 11 Coxa Vara Collared, REF 1...

The firm has identified that packaging containing components of the hip replacement range are mislabeled. This could result in the product intended to be used for a procedure not included in the packaging resulting in a surgical delay.

FDAOct 9, 2019CA• Signature Orthopaedics Europe Ltd Unit A, IDA Business & Technology Park Garrycastle Athlone Ireland

Amino Acid Injection (Nephron) – Sterility and Leak Risk (2019)

Lack of Assurance of Sterility; bags have potential to leak

Class IIModerate

FDAOct 9, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

PF-Fentanyl Citrate (Nephron) – Glass Contamination (2019)

GMP Deviations: potential glass contamination

Class IIModerate

FDAOct 9, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

del Nido Cardioplegia Solution (Nephron) – Sterility and Leak Risk (2019)

Lack of Assurance of Sterility; bags have potential to leak

Class IIModerate

FDAOct 9, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Rifampin Injection (Mylan) – Impurity Degradation (2019)

Failed Impurities/Degradation Specifications: discoloration due to elevated unknown impurity results which could decrease the effectiveness of the product.

Class IIModerate

FDAOct 7, 2019Nationwide• Mylan Laboratories Limited (Sterile Products Division)

Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom: Randox Liquid Cardiac Controls Catalogue Number CQ5051

Removal of claims for N-proBNP in the Liquid Cardiac Control model numbers CQ5051 due to an observed decrease in recovery for N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP) in recent lots.

FDAOct 4, 2019CA, CO, DE +7 more• Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom