Severity
Moderate
ModerateActive
CPSC recall · Reported August 26, 2020
Communicorp Recalls Plush Aflac Doctor Duck Due to Violation of Federal Lead Content Ban; Lead Poisoning Hazard
The buttons on the lab coat worn by the Doctor Duck contain levels of lead that exceed the federal lead content standard. Lead is toxic if ingested by young children and can cause…
Beverly Hills Teddy Bear Company, of Santa Clarita, Calif. recalled This recall involves the six inch plush Aflac promotional Doctor Duck. Doctor Duck is whi… - a moderate-severity action.
Communicorp Recalls Plush Aflac Doctor Duck Due to Violation of Federal Lead Content Ban;… was recalled by Beverly Hills Teddy Bear Company, of Santa Clarita, Calif. in August 26, 2020. Reason: The buttons on the lab coat worn by the Doctor Duck contain levels of lead that exceed the federal lead conte…. Remedy: Consumers should immediately dispose of the recalled plush Doctor Duck. Communicorp is co…. Verify recall #20173 with the CPSC before acting.
The recall
Beverly Hills Teddy Bear Company, of Santa Clarita, Calif. issued this moderate-severity CPSC recall-The buttons on the lab coat worn by the Doctor Duck contain levels of lead that exceed the federal lead conte….
- Moderate
- severity level
- August 26, 2020
- reported
Sourced from official CPSC enforcement records. Verify recall #20173 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #20173) was formally reported on August 26, 2020. It is classified under Moderate severity, with a current status of Active. Beverly Hills Teddy Bear Company, of Santa Clarita, Calif. is listed as the recalling firm. Federal records list the affected scope as About 635,500.
The documented reason for this recall is: The buttons on the lab coat worn by the Doctor Duck contain levels of lead that exceed the federal lead content standard. Lead is toxic if ingested by young children and can cause adverse health issues. 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 dispose of the recalled plush Doctor Duck. Communicorp is contacting Aflac employees and licensed agents who purchased the Doctor Duck directly. - 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, 6 from CPSC - 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 - 3,056 household products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
About 635,500
Related Recalls
6
6 from same agency
Product description
This recall involves the six inch plush Aflac promotional Doctor Duck. Doctor Duck is white with a yellow beak and feet. It is dressed in a white lab coat with buttons and a stethoscope. "Aflac" is printed on the front of the duck's lab coat. The plush ducks were distributed by Aflac to consumers as a promotional item.
Reason for recall
The buttons on the lab coat worn by the Doctor Duck contain levels of lead that exceed the federal lead content standard. Lead is toxic if ingested by young children and can cause adverse health issues.
Remedy, what to do
Consumers should immediately dispose of the recalled plush Doctor Duck. Communicorp is contacting Aflac employees and licensed agents who purchased the Doctor Duck directly.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 20173 |
| Date reported | August 26, 2020 |
| Date initiated | August 26, 2020 |
| Recalling firm | Beverly Hills Teddy Bear Company, of Santa Clarita, Calif. |
| Affected scope | About 635,500 |
| 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 dispose of the recalled plush Doctor Duck. Communicorp is contacting Aflac employees and licensed ag…
- Check the recall number (20173) 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 the six inch plush Aflac promotional Doctor Duck. Doctor Duck is white with a yellow beak and feet. It is dressed in a white lab coat with buttons and a stethoscope. "Aflac" is printed on the front of the duck's lab coat. The plush ducks were distributed by Aflac to consumers as a promotional item.. Recalled by Beverly Hills Teddy Bear Company, of Santa Clarita, Calif.. Units affected: About 635,500.
Why was this product recalled? ▼
The buttons on the lab coat worn by the Doctor Duck contain levels of lead that exceed the federal lead content standard. Lead is toxic if ingested by young children and can cause adverse health issues.
What should consumers do? ▼
Consumers should immediately dispose of the recalled plush Doctor Duck. Communicorp is contacting Aflac employees and licensed agents who purchased the Doctor Duck directly.
Which agency issued this recall? ▼
This recall was issued by the CPSC on August 26, 2020. Severity: Moderate. Recall number: 20173.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (20173) 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.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: CPSC, reported August 26, 2020. 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 July 2026.