Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100, H938690025, H93869025, H938693025, H938696025, H93868025, H93868100, H938672025, H938672100, H938675025, H938675100, H938678025, and H938678100.
FDA Recall Z-1227-2015 · Posted 2015-02-27
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Recalling FirmBaxter Corporation Englewood
Recall StatusTerminated
Product CodeKYX
Date Initiated2014-12-29
Date Terminated2016-08-08
Product Quantity1,404,230
Reason for Recall
Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.
Firm Action
Baxter sent an Safety Alert letter dated January 15, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
Baxter is requesting that you take the following actions:
1.Complete the enclosed customer reply form and return it to Baxter by faxing it to 224-270-5457 or scanning and e-mailing it to [email protected]. Returning the customer reply form promptly will prevent you from receiving repeat notices.
2. Please forward a copy of this Safety Alert letter to other facilities or departments within your institutions to ensure that those locations are aware of this action.
Action to be taken if you are an end-user and purchased product from a distributor or reseller:
1. Please forward a copy of this Safety Alert letter to other facilities or departments within your institutions to ensure that those locations are aware of this action.
2. Follow your supplier's reply process. Please do not return the customer reply form to Baxter.
Action to be taken if you are a distributor:
If you are a dealer, wholesaler, or distributor/reseller that distributed any product to other facilities, please notify your customers of this Safety Alert in accordance with your customary procedures. Further information and support
For general questions regarding this communication, contact The Center for One Baxter at 800-422-9837, Monday through Friday, between the hours of 8:00 AM and 5:00 PM Central Time.
Root Cause
Labeling Change Control
Distribution Pattern
Nationwide Distribution
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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