Abbott Laboratories, Inc Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening, plasma and plasmapheresis screening, and organ donor centers, hospitals, and reference laboratories. Recall
Hazard assessment based on recall description.
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
Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening, plasma and plasmapheresis screening, and organ donor centers, hospitals, and reference laboratories.
Brand
Abbott Laboratories, Inc
Lot Codes / Batch Numbers
Model Number: LN 06P16-01 Serial numbers AS1001 through AS1330
Products Sold
Model Number: LN 06P16-01 Serial numbers AS1001 through AS1330
Abbott Laboratories, Inc is recalling Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in bl due to A design defect (hardware and software) allows liquid waste pressure to build up and potentially spray users/operators.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A design defect (hardware and software) allows liquid waste pressure to build up and potentially spray users/operators.
Recommended Action
Per FDA guidance
On 07/12/2021, the firm started hand-delivering an "Product Correction Urgent-Immediate Action Required" Notification to customers informing them that the Recalling Firm has identified an issue with pressure build up in the external waste tubing of the liquid waste assembly system if obstructed leading to a potential for biohazardous exposure and/or operator injury (contact with liquid waste). Customers are instructed to follow the below instruction until the Recalling Firm can upgrade the analyzers with a future system software version and a hardware component: 1. As stated in Section 8, Hazards, follow all product labeling and safety instructions in the laboratory. Always wear personal protective equipment (PPE) when operating the analyzer system, other laboratory instrumentation and equipment, and when using chemicals. 2. Adhere to the instructions listed in the Operations Manual, Section 10, to resolve message codes pertaining to waste overflow and contact Customer Service to resolve issues related to hardware failure. 3. Use caution when handling the Alinity s System external waste tubing. Avoid any configuration that could impact the free flow of the external waste and cause pressure buildup within the external waste tubing. A future software update and associated hardware upgrade will be implemented to enable external liquid waste tubing pressure monitoring and the display of the expected message code 5101 Liquid waste high pressure detected. 4. If customers have forwarded the product listed above to other laboratories, please inform them of this Product Correction and provide to them a copy of this letter. 5. Complete and return the Customer Reply form. 6. Retain this letter for their laboratory records. If customers or any of the health care providers have questions regarding this information, U.S. Customers contact Customer Service at 1-877-4ABBOTT (available 24 hours a day, 7 days a week). Customers outside the U.S., please contact your local area Cust
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