Severity
Moderate
ModerateActive
CPSC recall · Reported February 6, 2020
Country Home Products Recalls DR Walk Behind Leaf Blowers Due to Projectile Hazard
The blades inside the leaf blower can break off and discharge from the unit, posing a projectile hazard to the user or bystanders.
The recall
Country Home Products Inc., d/b/a Dr Power Equipment, of South Burlington, Vt. issued this moderate-severity CPSC recall — The blades inside the leaf blower can break off and discharge from the unit, posing a projectile hazard to th….
- Moderate
- severity level
- February 6, 2020
- reported
Sourced from official CPSC enforcement records. Verify recall #20070 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #20070) was formally reported on February 6, 2020. It is classified under Moderate severity, with a current status of Active. Country Home Products Inc., d/b/a Dr Power Equipment, of South Burlington, Vt. is listed as the recalling firm. Federal records list the affected scope as About 100.
The documented reason for this recall is: The blades inside the leaf blower can break off and discharge from the unit, posing a projectile hazard to the user or bystanders. 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 leaf blowers and contact the firm for instructions to receive a full refund. — consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Household Products recalls over time
Where this recall sits in its category — 2,542 household products recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Affected scope
About 100
Related Recalls
6
0 from same agency
Product description
This recall involves DR Walk Behind Leaf Blowers, including DR PREMIER 1200, DR PRO 2000 and DR PRO 2000SP. The blowers are three-wheeled walk behind blowers with an orange circular metal face with a black center with "DR" printed on the front. The model number is printed on the front left side of the main impeller housing and on the serial number label located on the back right side of the main impeller housing. Only the following models are included in the recall: Product name Model Number DR PREMIER 1200 Walk Behind Leaf Blower WB13010DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DEN DR PRO 2000SP Walk Behind Leaf Blower WB17020DEN
Reason for recall
The blades inside the leaf blower can break off and discharge from the unit, posing a projectile hazard to the user or bystanders.
Remedy — what to do
Consumers should immediately stop using the recalled leaf blowers and contact the firm for instructions to receive a full refund.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 20070 |
| Date reported | February 6, 2020 |
| Date initiated | February 6, 2020 |
| Recalling firm | Country Home Products Inc., d/b/a Dr Power Equipment, of South Burlington, Vt. |
| Affected scope | About 100 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately stop using the recalled leaf blowers and contact the firm for instructions to receive a full refund.
- Check the recall number (20070) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
This recall involves DR Walk Behind Leaf Blowers, including DR PREMIER 1200, DR PRO 2000 and DR PRO 2000SP. The blowers are three-wheeled walk behind blowers with an orange circular metal face with a black center with "DR" printed on the front. The model number is printed on the front left side of the main impeller housing and on the serial number label located on the back right side of the main impeller housing. Only the following models are included in the recall: Product name Model Number DR PREMIER 1200 Walk Behind Leaf Blower WB13010DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DEN DR PRO 2000SP Walk Behind Leaf Blower WB17020DEN. Recalled by Country Home Products Inc., d/b/a Dr Power Equipment, of South Burlington, Vt.. Units affected: About 100.
Why was this product recalled? ▼
The blades inside the leaf blower can break off and discharge from the unit, posing a projectile hazard to the user or bystanders.
What should consumers do? ▼
Consumers should immediately stop using the recalled leaf blowers and contact the firm for instructions to receive a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on February 6, 2020. Severity: Moderate. Recall number: 20070.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (20070) 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.
Continue exploring
Keep tracking product safety across the federal recall archive.
Recall Checker
Search the full archive by product name, brand, or recall number across every agency.
Check a product →
CPSC recalls
Every recall issued by CPSC, newest first.
Browse the feed →
RecallRadar
Live feed of the latest recalls across the FDA, CPSC and NHTSA — filter by agency and severity.
View the live feed →
Rankings
The largest recalls by units affected and the most-recalled product categories.
See the rankings →
Browse by category
Find recalls by product type to spot recurring defect patterns.
All categories →
What to do next
A step-by-step guide to refunds, repairs, and returns after a recall.
Read the guide →
Nearby Recalls in This Category
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
FDA Food Moderate
Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master case of 2 Kg (4.41 lb) each total case wei…
Disaronno Ingredients S.p.a. · 2026-05-13
FDA Drug Moderate
Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054,…
Wells Pharma of Houston LLC · 2026-05-06
FDA Drug Moderate
fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, ND…
Wells Pharma of Houston LLC · 2026-05-06
FDA Drug Moderate
fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride, Narcotic, (2500 mcg/ 250 mL) (10 mcg per mL), 250 mL bag,…
Wells Pharma of Houston LLC · 2026-05-06
FDA Drug Moderate
fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houst…
Wells Pharma of Houston LLC · 2026-05-06
Compare this recall with Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed … →
Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported February 6, 2020.
- 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)
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.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.