Cook Inc.: Medical Device Recall in 2019 - (Recall #: Z-1722-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Pericardiocentesis Catheter Set, RPN C-PCS-850, Order # G03282

Product Classification:

Class II

Date Initiated: April 9, 2019

Date Posted: June 12, 2019

Recall Number: Z-1722-2019

Event ID: 82692

Reason for Recall:

Affected products may have been manufactured with the catheter distal end hole too small

Status: Terminated

Product Quantity: 83 kits

Code Information:

Lot Numbers 7716007 7703324 NS7703501 NS7703502 NS7703503 NS7704718 NS7704722 NS7704727 NS7704728

Distribution Pattern:

Domestically: OH; Internationally: CANADA, SPAIN, ITALY, BELGIUM, GERMANY, UNITED ARAB EMIRATES, GREECE, SWITZERLAND, OMAN, MONACO, SAUDI ARABIA, AUSTRALIA, HONG KONG, INDIA & KOREA

Voluntary or Mandated:

Voluntary: Firm initiated