Severity
Moderate
ModerateActive
CPSC recall · Reported April 29, 2014
DGL Group Recalls Vibe USB Mobile Power Bars Due to Fire Hazard; Sold Exclusively at Five Below
The power bar can overheat, posing a fire hazard.
The CPSC recalled This recall involves Vibe USB mobile power bars also known as portable USB power supply o… — a moderate-severity action.
DGL Group Recalls Vibe USB Mobile Power Bars Due to Fire Hazard; Sold Exclusively at Five… was recalled and listed by the CPSC in April 29, 2014. Reason: The power bar can overheat, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled power bar, unplug it from the electr…. Verify recall #14162 with the CPSC before acting.
The recall
issued this moderate-severity CPSC recall — The power bar can overheat, posing a fire hazard..
- Moderate
- severity level
- April 29, 2014
- reported
Sourced from official CPSC enforcement records. Verify recall #14162 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #14162) was formally reported on April 29, 2014. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records list the affected scope as About 99,000.
The documented reason for this recall is: The power bar can overheat, posing a fire hazard. 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 power bar, unplug it from the electrical outlet and return it to the DGL Group for a full refund and a $5 coupon towards another purchase at Five … — 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.
Medical Devices recalls over time
Where this recall sits in its category — 40,409 medical devices 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.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
About 99,000
Related Recalls
6
0 from same agency
Product description
This recall involves Vibe USB mobile power bars also known as portable USB power supply or portable chargers. The power bars were sold in black, white, blue, green, pink and purple. The rectangular-shaped power bars measure one square inch by three inches long and have a cord with key ring attached at the end. "Power Bank" is embossed on the face of the device. "Vibe" and "Power Bar" are printed on the front of the black packaging along with an image of the device in one of the six colors. Model number FB-Bar is printed below the UPC code on the bottom of the packaging
Reason for recall
The power bar can overheat, posing a fire hazard.
Remedy — what to do
Consumers should immediately stop using the recalled power bar, unplug it from the electrical outlet and return it to the DGL Group for a full refund and a $5 coupon towards another purchase at Five Below.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 14162 |
| Date reported | April 29, 2014 |
| Date initiated | April 29, 2014 |
| Recalling firm | Not disclosed |
| Affected scope | About 99,000 |
| 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 power bar, unplug it from the electrical outlet and return it to the DGL Gro…
- Check the recall number (14162) 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 Vibe USB mobile power bars also known as portable USB power supply or portable chargers. The power bars were sold in black, white, blue, green, pink and purple. The rectangular-shaped power bars measure one square inch by three inches long and have a cord with key ring attached at the end. "Power Bank" is embossed on the face of the device. "Vibe" and "Power Bar" are printed on the front of the black packaging along with an image of the device in one of the six colors. Model number FB-Bar is printed below the UPC code on the bottom of the packaging. Units affected: About 99,000.
Why was this product recalled? ▼
The power bar can overheat, posing a fire hazard.
What should consumers do? ▼
Consumers should immediately stop using the recalled power bar, unplug it from the electrical outlet and return it to the DGL Group for a full refund and a $5 coupon towards another purchase at Five Below.
Which agency issued this recall? ▼
This recall was issued by the CPSC on April 29, 2014. Severity: Moderate. Recall number: 14162.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (14162) 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 Devices Moderate
GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used i…
GE Medical Systems Information Technologies Inc · 2026-06-03
FDA Devices Critical
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit…
Medline Industries, LP · 2026-06-03
FDA Devices Critical
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Med…
Medline Industries, LP · 2026-06-03
FDA Devices Critical
Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella C…
Abiomed, Inc. · 2026-06-03
FDA Devices Moderate
GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCA…
GE Medical Systems Information Technologies Inc · 2026-06-03
Compare this recall with GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L… →
Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported April 29, 2014.
- 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.