PlainRecalls

Applica Consumer Products Reannounces Black & Decker Spacemaker Coffeemaker Recall Due to Injury Hazard; Units Sold After Recall

Reported: August 15, 2013 Initiated: August 15, 2013 #13267 About 641; (159,000 units were recalled in June 2012) units

Applica Consumer Products Inc. of Miramar, Fla. issued this CPSC recall on August 15, 2013. Classified as Moderate severity. Approximately About 641; (159,000 units were recalled in June 2012) units are affected. The recall was issued because: The coffee pot handle can break, causing cuts and burns to the consumer.. 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 #13267) was formally reported on August 15, 2013. It is classified under Moderate severity, with a current status of Active. Applica Consumer Products Inc. of Miramar, Fla. is listed as the recalling firm. Federal records indicate About 641; (159,000 units were recalled in June 2012) 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 coffee pot handle can break, causing cuts and burns to the consumer. 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 coffeemakers and contact Applica for a full refund of the under-the-counter coffeemaker. — 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 13 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 641; (159,000 units were recalled in June 2012)

Related Recalls

6

0 from same agency

Product Description

The recalled coffee maker is designed to mount under a cabinet. It is available in white or black and has the words "BLACK and DECKER® SPACEMAKER™" printed in the top right-hand corner of the product. The coffeemakers have a digital time display in the top left corner and five round buttons above the water reservoir for programming. The 12-cup coffee pots are glass with a molded handle the same color as the machine and a silver metallic bracket running around the glass near the bottom. The model number is printed on the underside of the coffeemaker, directly below the water reservoir. Model number SDC 740 was previously recalled with other eight models in 2012. After the recall announcement, an additional 641 units continued to be sold.

Reason for Recall

The coffee pot handle can break, causing cuts and burns to the consumer.

Remedy

Consumers should immediately stop using the coffeemakers and contact Applica for a full refund of the under-the-counter coffeemaker.

Details

Units Affected
About 641; (159,000 units were recalled in June 2012)

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 13267
Date reported August 15, 2013
Date initiated August 15, 2013
Recalling firm Applica Consumer Products Inc. of Miramar, Fla.
Units affected About 641; (159,000 units were recalled in June 2012)
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 641; (159,000 units were recalled in June 2012) 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?
The recalled coffee maker is designed to mount under a cabinet. It is available in white or black and has the words "BLACK and DECKER® SPACEMAKER™" printed in the top right-hand corner of the product. The coffeemakers have a digital time display in the top left corner and five round buttons above the water reservoir for programming. The 12-cup coffee pots are glass with a molded handle the same color as the machine and a silver metallic bracket running around the glass near the bottom. The model number is printed on the underside of the coffeemaker, directly below the water reservoir. Model number SDC 740 was previously recalled with other eight models in 2012. After the recall announcement, an additional 641 units continued to be sold.. Recalled by Applica Consumer Products Inc. of Miramar, Fla.. Units affected: About 641; (159,000 units were recalled in June 2012).
Why was this product recalled?
The coffee pot handle can break, causing cuts and burns to the consumer.
What should consumers do?
Consumers should immediately stop using the coffeemakers and contact Applica for a full refund of the under-the-counter coffeemaker.
Which agency issued this recall?
This recall was issued by the CPSC on August 15, 2013. Severity: Moderate. Recall number: 13267.
How do I check if my product is affected by a recall?
Check the product description and recall number (13267) 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.

Compare this recall with Endo-Model Replacement Plateau; Item Number: 15-0027/11; →

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).