PlainRecalls

Nutrilife Recalls Bottles of Hydrogen Peroxide Due to Fire, Burn Hazards

Reported: August 23, 2017 Initiated: August 23, 2017 #17209 About 11,800 (in addition, about 3,500 in Canada) units

Nutrilife Plant Products, of Canada issued this CPSC recall on August 23, 2017. Classified as Moderate severity. Approximately About 11,800 (in addition, about 3,500 in Canada) units are affected. The recall was issued because: The bottle caps on the 29% hydrogen peroxide one-gallon bottles do not vent properly and can allow pressure to build up…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This CPSC action (record #17209) was formally reported on August 23, 2017. It is classified under Moderate severity, with a current status of Active. Nutrilife Plant Products, of Canada is listed as the recalling firm. Federal records indicate About 11,800 (in addition, about 3,500 in Canada) units are affected, placing this recall in the million-unit bracket that typically triggers nationwide consumer alerts and retailer sweeps.

The documented reason for this recall is: The bottle caps on the 29% hydrogen peroxide one-gallon bottles do not vent properly and can allow pressure to build up in the bottle and cause it to expand and rupture, posing fire and burn hazards. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately stop using the recalled bottles of hydrogen peroxide, contact Nutrilife for safe handling instructions and to receive a free replacement bottle cap or for instructions on… — consumers holding this product should act on that instruction rather than relying on general guidance.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 9 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

About 11,800 (in addition, about 3,500 in Canada)

Related Recalls

6

0 from same agency

Product Description

This recall involves Nutrilife Plant Products one-gallon/four-liter bottles of hydrogen peroxide (H202) liquid 29% oxidizer which is used as a source of oxygen for water, a preservative for fresh cut flowers, and to keep unwanted nutrient residuals clear in reservoirs, drippers and dripper lines. The plastic bottles are white with a blue/green label with a handle at the top. The Nutrilife logo, H202, Liquid 29% Oxidizer and "An Oxygen Source for Water" are printed on the front label. Open and closing instructions are printed on the bottle caps with indented lettering.

Reason for Recall

The bottle caps on the 29% hydrogen peroxide one-gallon bottles do not vent properly and can allow pressure to build up in the bottle and cause it to expand and rupture, posing fire and burn hazards.

Remedy

Consumers should immediately stop using the recalled bottles of hydrogen peroxide, contact Nutrilife for safe handling instructions and to receive a free replacement bottle cap or for instructions on how to destroy the bottles and receive a full refund.

Details

Units Affected
About 11,800 (in addition, about 3,500 in Canada)

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 17209
Date reported August 23, 2017
Date initiated August 23, 2017
Recalling firm Nutrilife Plant Products, of Canada
Units affected About 11,800 (in addition, about 3,500 in Canada)
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 11,800 (in addition, about 3,500 in Canada) units affected — million-unit bracket.

Regional (<10K units)
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units) ✓ This recall

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

Frequently Asked Questions

What product was recalled?
This recall involves Nutrilife Plant Products one-gallon/four-liter bottles of hydrogen peroxide (H202) liquid 29% oxidizer which is used as a source of oxygen for water, a preservative for fresh cut flowers, and to keep unwanted nutrient residuals clear in reservoirs, drippers and dripper lines. The plastic bottles are white with a blue/green label with a handle at the top. The Nutrilife logo, H202, Liquid 29% Oxidizer and "An Oxygen Source for Water" are printed on the front label. Open and closing instructions are printed on the bottle caps with indented lettering.. Recalled by Nutrilife Plant Products, of Canada. Units affected: About 11,800 (in addition, about 3,500 in Canada).
Why was this product recalled?
The bottle caps on the 29% hydrogen peroxide one-gallon bottles do not vent properly and can allow pressure to build up in the bottle and cause it to expand and rupture, posing fire and burn hazards.
What should consumers do?
Consumers should immediately stop using the recalled bottles of hydrogen peroxide, contact Nutrilife for safe handling instructions and to receive a free replacement bottle cap or for instructions on how to destroy the bottles and receive a full refund.
Which agency issued this recall?
This recall was issued by the CPSC on August 23, 2017. Severity: Moderate. Recall number: 17209.
How do I check if my product is affected by a recall?
Check the product description and recall number (17209) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product?
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).