LVP Primary Administration Set (Cypress Medical) – Medication Flow Risk (2024)
Syringes lack FDA clearance and were inadvertently shipped due to an internal processing error.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Number: 102-S60C
Brand
Cypress Medical Products LLC
Lot Codes / Batch Numbers
UDI-DI: 20612479170302
Products Sold
UDI-DI: 20612479170302;
Cypress Medical Products LLC is recalling General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson due to The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes l. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error.
Recommended Action
Per FDA guidance
An Urgent Product Recall Notification letter dated 8/6/24 was sent to customers. Actions to be Taken 1. Immediately quarantine and discontinue use of any product matching the affected items and lot numbers listed above. Affected items should be destroyed on location per appropriate local, state, and federal disposal requirements. 2. Please complete and return the enclosed response form (Attachment #1) as soon as possible, even if you do not have any product on hand or have already consumed the product. Return completed form to MMSQRCProductReviews@Mckesson.com. 3. If you have further distributed this product to end users, please notify them immediately of this urgent product recall and ask them to segregate and quarantine this product immediately. You are encouraged to include a copy of this notification letter in your communication with any of these end users. If you have questions regarding this notification, please contact McKesson directly by phone at (800) 688-8840 or email MMSQRCProductReviews@Mckesson.com. Representatives are available Monday Friday, 8:00 am 5:00 pm PST.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026