PlainRecalls
CPSC Moderate Active

Coravin Recalls to Repair Wine Access System Due to Laceration Hazard

Reported: June 25, 2014 Initiated: June 25, 2014 #14214

Product 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.

Reason for Recall

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.

Details

Units Affected
About 65,000 in the U.S. and about 640 in Canada
Official Source
https://www.cpsc.gov/Recalls/2014/Coravin-Recalls-to-Repair-Wine-Access-System

Frequently Asked Questions

What product was recalled? ▼
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.. Units affected: About 65,000 in the U.S. and about 640 in Canada.
Why was this product recalled? ▼
The system can cause wine bottles to break during pressurization, posing a risk of lacerations.
What should consumers do? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 25, 2014. Severity: Moderate. Recall number: 14214.

Related Recalls

FDA Drug Moderate

Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle, Rx Only, Manufactured by: U…

Unichem Pharmaceuticals USA Inc. · 2026-02-11
FDA Drug Critical

Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San…

Green Lumber Holdings, LLC · 2026-02-11
FDA Drug Moderate

Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500…

Granules Pharmaceuticals Inc. · 2026-02-11
FDA Drug Critical

Diclofenac Sodium, Topical Gel, 3%, 100 g, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1…

SUN PHARMACEUTICAL INDUSTRIES INC · 2026-02-11
FDA Drug Critical

Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt. Ltd., Ahmedabad, India UPC 8 904218 700313

HANDELNINE GLOBAL LLC · 2026-02-11

Explore Related Data

Vehicle Safety → Drug Information →