RecallDepth

Accessory Kit, Catalog#10282965, #10373217,#10286080. The Immulite 2000 systems are continuous random-access instruments that perform chemiluminescent immunoassays. These instruments use serum, plasma, or urine samples for in vitro diagnostic testing.

This recall has been terminated (originally issued May 23, 2015).

Company
Siemens Medical Solutions Diagnostics
Recall Initiated
March 5, 2015
Posted
May 23, 2015
Terminated
January 16, 2018
Recall Number
Z-1660-2015
Quantity
962 bottles
Firm Location
Flanders, NJ
Official Source
View on FDA website ↗

Reason for Recall

The bottle assemblies were manufactured with a quality issue where in some cases the smaller diameter opening on both IMMULITE 2000 and IMMULITE 2000XPi Water Bottles and Liquid Waste Bottles is undersized and/or deformed, preventing the cap from closing or fastening securely to the bottle.

Distribution

Worldwide Distribution.

Lot / Code Info

Accessory Kit - Product Code/Catalog #'s 10282965, 10373217 and 10286080

Root Cause

Nonconforming Material/Component

Action Taken

Siemens Healthcare Diagnostics sent an Urgent Device Correction Letter/Field Correction Effective Check Form dated 3/5/15 via FedEx to their affected customers.

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