Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels
FDA device recall Z-0958-2023 · posted 2023-01-17 · Open, Classified
Recall details
- Recalling firm
- Abbott Laboratories
- Reason for recall
- Reaction vessels may contain a potential contaminant that could affect their optical performance.
- Action taken
- On 11/24/22, the recalling firm phoned customers and informed them of the recall using a phone script. On the same day, the phone call was followed by an email that restated the information in the phone script and included a Customer Reply form. Customers were asked to discontinue use and destroy the impacted inventory according to their laboratory procedures. If customers forwarded the product to other laboratories, they were asked to inform them of this Product Recall and complete and return the Customer Reply form, which can be returned to PMS@abbott.com. The reply form asked customers to record the number of boxes destroyed. If you have any questions, contact QA Manager, Post Market Surveillance at 224-668-0343 or email: suchin.song@abbott.com.
- Root cause
- Material/Component Contamination
- Status
- Open, Classified
- Product code
- DHA
- Quantity affected
- 70 cases
- Distribution
- US Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WV
- Date initiated
- 2022-11-24
- Date posted
- 2023-01-17
- Location
- Irving, TX
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| Alinity i Total ß-hCG Reagent Kit, Alinity i System (K170317) | Abbott Laboratories | 2017-10-23 |