C.R. Bard, Inc., Urological Division: Medical Device Recall in 2012 - (Recall #: Z-2327-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for single use. Used to catheterize patients. The finished trays are sold in Tyvek breather bags.

Product Classification:

Class II

Date Initiated: June 29, 2012

Date Posted: September 19, 2012

Recall Number: Z-2327-2012

Event ID: 62774

Reason for Recall:

Incomplete seal on sterile packages of product.

Status: Terminated

Product Quantity: 56,694 units

Code Information:

Catalog No. 300316A (Lot Nos. - NGVJ1108, NGVJ1712, NGVJ1713, NGVJ1105, NGVJ1714) Catalog No. 898316 (Lot Nos. NGVJ1614, NGVJ1615, NGVJ1616, NGVJ1617) Catalog No. 897414 (Lot No. NGVJ1705) Catalog No. 907618 (Lot No. NGVJ1757) Catalog No. 907600 (Lot No. NGVJ1764)

Distribution Pattern:

Nationwide distribution: USA

Voluntary or Mandated:

Voluntary: Firm initiated