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  4. ICU Medical Issues a Voluntary Nationwide Recall of Certain Lots of Plum and Sapphire Microbore Infusion Sets with Inline Filters
  1. Recalls, Market Withdrawals, & Safety Alerts

COMPANY ANNOUNCEMENT

ICU Medical Issues a Voluntary Nationwide Recall of Certain Lots of Plum and Sapphire Microbore Infusion Sets with Inline Filters

When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company.

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Summary

Company Announcement Date:
FDA Publish Date:
Product Type:
Medical Devices
Reason for Announcement:
Recall Reason Description
Potential for small amounts of fluid leaking out of the air vents on the inline filters
Company Name:
ICU Medical, Inc.
Brand Name:
Brand Name(s)
Plum and Sapphire
Product Description:
Product Description
Microbore Infusion Sets

Company Announcement

ICU Medical, Inc. announced a voluntary recall on 29 July 2019 of certain lots of Plum and Sapphire Microbore Infusion Sets with inline filters due to the potential for small amounts of fluid leaking out of the air vents on the inline filters. To date, ICU Medical is not aware of adverse events related to this matter and is issuing this notification out of an abundance of caution.

Based on complaints the affected product lots, which were distributed nationwide to ICU Medical customers, are listed below:

Item Code Product Description - PlumSets Lot #
118790412 High-Pressure Filter PRIMARY I.V. PLUMSET Convertible Pin, 104 Inch with Orange Polyethylene-Lined*/Light Resistant Tubing, Prepierced Injection Site and OPTION-LOK 855505H, 865135H, 918695H, 928085H, 937325H, 3864774, 3935434, 4011065, 4088425
142560488 Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch 865455H, 896215H, 897455H, 3864785, 4095291
149530489 Primary PLUM Set Yellow Striped Tubing, Distal Microbore Tubing, 0.2 Micron Filter, Secure Lock, 107 Inch 925155H
Item Code Product Description - Sapphire Sets Lot#
163350455 SAPPHIRE Primary 1.2 Micron Filter Set Microbore, 122 Inch 855935H, 855965H, 876145H, 885395H, 896135H, 936605H, 3843263, 3864786
163620455 SAPPHIRE Primary 0.2 Micron Filter Set, Microbore, CLAVE Y-Site, 118 Inch 855645H, 885415H, 896625H, 4008547
163630455 SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch 876175H, 885385H, 896995H, 908235H, 925755H, 3843264
163730455 SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter, PAV 123 inch 896225H, 916845H, 925825H
948155H
163830455 SAPPHIRE Primary 0.2 Micron Filter Set Non-Vented, Microbore, PAV, CLAVE Y-Site, 122 Inch 855665H, 865495H, 896195H
3849197, 4064964
163840455 SAPPHIRE Primary 1.2 Micron Filter Set Non-Vented, Microbore, PAV, 123 Inch 855995H, 865505H, 876185H
240100401 SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch 897525H, 905915H, 926235H

Customers with questions regarding this recall can call ICU Medical at 1-866-829-9025 option 8, Monday through Friday, between the hours of 8 a.m. and 6 p.m. Central Time.

If the benefits of a filtered microbore infusion set are greater than the potential risks of a filter leak (as described below), please review the customer notification for additional details regarding actions required by the user.

As of the date of this press release, FDA is actively evaluating the information in an effort to classify this recall. Fluid leakage may potentially cause delay of infusion, medication under-delivery, contamination of the fluid path which is on the patient side of the filter, exposure to hazardous medications, or fluid path air-in-line. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

  • Complete and submit the report Online
  • Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Additional information regarding this recall, along with notifications to the customer can be found on ICU Medical’s Website here.


Company Contact Information

Consumers:
1-866-829-9025 option 8
Media:
Tom McCall
949-366-4368
tmccall@icumed.com