Wine Access System
Class III - Low RiskWhat Should You Do?
- Check if you have this product: (About 65,000 in the U.S. and about 640 in Canada)
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
Recall Details
- Company:
- Unknown Manufacturer
- Reason for Recall:
- The system can cause wine bottles to break during pressurization, posing a risk of lacerations.
- Classification:
- Class III - Low Risk
Products that are unlikely to cause any adverse health reaction, but violate FDA regulations.
- Status:
- ongoing
- Hazard:
- The system can cause wine bottles to break during pressurization, posing a risk of lacerations.
- Remedy:
- Consumers should immediately stop using the recalled wine access system and contact Coravin for a free repair kit that includes a neoprene wine bottle sleeve to contain broken glass when a bottle breaks and updated instructions and warnings. The wine access system should not be used on wine bottles with damages or flaws.
Product Images
Product Information
Full Description:
This recall involves all Coravin™ 1000 Wine Access Systems. The system uses a hollow needle to penetrate a wine bottle cork and allow wine to be dispensed without removing the cork. The system is about nine inches tall and has a silver-colored, metallic tubular body with a detachable black plastic capsule cup attached to the bottom and trigger on the top. A black metal handle is attached at the top of the tube and a black metal, moveable bottle clamp is attached to the front side of the tube. A long, metallic needle protrudes from the underside of the handle. The Coravin name and logo appear on the front side of the tube. The system comes with a silver-colored storage base and two argon gas capsules.
Product Codes/Lot Numbers:
(About 65,000 in the U.S. and about 640 in Canada)
Official Source
Always verify recall information with the official CPSC source:
View on CPSC.govCPSC Recall Number: 14214
Related Recalls
AMP MP2 Smart Fitness Machine
Unknown Manufacturer
The arm on the MP2 model of the fitness machine does not lock properly, which can allow the arm to swing unexpectedly, posing a risk of laceration or serious injury.
ANNQUAN Power Strips, Models EX-D112-05 and EX-D106-25
Unknown Manufacturer
The power strips do not contain supplementary overcurrent protection, which creates a risk of fire if the power strips are overloaded. The resulting fire can cause serious injury or death from smoke inhalation and burns.
Blue Wave brand 48-inch and taller above-ground pools
Unknown Manufacturer
The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk.