Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

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 ↗

Home
/
Brands
/
Schwabe North America, Inc.

Schwabe North America, Inc. Recalls

All product recalls associated with Schwabe North America, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

590

Class I (Serious)

65

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 8021–8040 of 10391 recalls

Alive No Iron (Nature's Way) – Enzyme Issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

Alive Women's Ultra Potency (Nature's Way) – Enzyme Issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

Phyto-Energizer Capsules (Nature's Way) – Enzyme Issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

1...400 401402403 404...520

Page 402 of 520Next

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

Alive Whole Food Energizer (Nature's Way) – Enzyme Issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

Alive Whole Food Energizer (Nature's Way) – Enzyme Issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

Alive Whole Food Energizer (Nature's Way) – Enzyme Issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

GL Completia Vcaps (Schwabe North America) – enzyme blend issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

Alive Men's Energizer (Nature's Way) – Enzyme Issue (2013)

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Class IIModerate

FDAOct 23, 2013AL, AK, AZ +44 more• Schwabe North America, Inc.

2011 CHEETAH 20-40 FT MAXIMIZER Recall: STRUCTURE

Cheetah Chassis Corporation (Cheetah) is recalling certain model year 2010-2014 20-40 Maximizer trailers manufactured September 14, 2009, through October 3, 2013. In the affected trailers, the weld joining the locator pin's shaft and collar may fail leading to a separation of the locating pin's shaft and collar.

NHTSAOct 17, 2013Nationwide• CHEETAH

Albuterol Sulfate Inhalation (Nephron) – Sterility Concern (2013)

Lack of Assurance of Sterility: Nephron Pharmaceuticals Corporation conducted a routine periodic aseptic process simulation and discovered bacterial growth in a number of media fill vials, exceeding the allowable limit.

Class IIModerate

FDAOct 2, 2013Nationwide• Nephron Pharmaceuticals Corp.

Potassium Chloride Tablets (Cardinal) – Incorrect Labeling (2013)

Labeling: Incorrect or Missing Package Insert: the package insert for the potassium chloride 8 mEq and 10 mEq strength instead of the potassium chloride 10 mEq and 20 mEq strength was packaged with the product.

FDAOct 2, 2013OK• Cardinal Health

Virilis Pro Capsules (Haute Health) – Unapproved Ingredients (2013)

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

FDASep 27, 2013Nationwide• Haute Health, LLC

PHUK Sexual Enhancement (Haute Health) – Unapproved Ingredients (2013)

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

FDASep 27, 2013Nationwide• Haute Health, LLC

Prolifta Supplement (Haute Health) – Unapproved Ingredients (2013)

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of an active ingredient found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

FDASep 27, 2013Nationwide• Haute Health, LLC

Black Cumin Seed Supplement (Swanson) – lot contamination (2013)

Swanson Health Products is recalling two lots of Swanson Premium Full Spectrum Black Cumin Seed (Nigella sativa) Dietary Supplement Capsules. The product was found to be mislabel. Bottles of Black Cumin Seed from these two lots numbers (199399 & 201359) have been found to contain White Cumin Seed (Cuminum cyminum).

FDASep 26, 2013Nationwide• Swanson Health Products, Inc

Acanya Gel (Valeant) – Incorrect Expiration Date (2013)

Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being carried out due to an incorrect expiration date assigned to a lot of physicians samples.

FDASep 20, 2013Nationwide• Valeant Pharmaceuticals North Am

GABA Supplement (Source Naturals) – metal fragment risk (2013)

The firm found small piece of metal fragment in one tablet during its inspection process.

Class IIModerate

FDASep 20, 2013Nationwide• Threshold Enterprises Ltd

Estradiol Progesterone Injectable (Apothecary Shoppe) – Sterility Risk (2013)

Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory.

Class IIModerate

FDASep 6, 2013OK• Apothecary Shoppe

Motrin Infants' Drops (McNeil) – Foreign Substance Presence (2013)

Presence of Foreign Substance: process-related particulates which may be associated with the raw materials were observed

Class IIModerate

FDASep 6, 2013Nationwide• Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc.

Testosterone Cypionate Injectable (Apothecary Shoppe) – Sterility Risk (2013)

Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory

Class IIModerate

FDASep 6, 2013OK• Apothecary Shoppe