Drug recall

Covidien Curity Eye Pad Item Code: 03201 The sterile eye pad is a device that consists of a pad made of…

FDA recall event 76606 · Class II · Covidien LLC

Key facts

Event ID 76606
Recall numbers Z-1739-2017, Z-1740-2017, Z-1741-2017, Z-1742-2017, Z-1743-2017, Z-1744-2017, Z-1745-2017
Recalling firm Covidien LLC
Product type Devices
Products Covidien Curity Eye Pad Item Code: 03201 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for…, Covidien Curity Eye Pad Item Code: 91650 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for…, Covidien Curity Eye Pad Oval, 1-5/8 x 2-5/8 (4.2 cm x 6.7 cm), Sterile Item Code: 2841 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton…, Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm), Sterile Item Code: 3606 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help…, Covidien Curity Sodium Chloride Dressing , 6 x 6-3/4 (15.2 cm x 17.1 cm), Sterile Item Code: 3339 Curity Sodium Chloride Dressing is indicated for use on exudating and/or infected wounds and 2 more
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Product sterility is compromised due to breach of sterile barrier
Initiation date Mar 3, 2017
Report date Apr 12, 2017
Termination date Oct 7, 2019
City North Haven
State CT
Country United States
FEI number 1219930

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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