Becton Dickinson & Co. recalls BD COR System Software. Model Number: 444829.
Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.
Read the official notice →- Date
- 2025-07-30
- Country
- United States
- Brand
- Becton Dickinson &
- Product
- BD COR System Software. Model Number: 444829.
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of Florida, Texas and…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Becton Dickinson & recalls
- 2025-11-26
US
Becton Dickinson & Company recalls BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
FDA · DeviceBecton Dickinson & CompanyWorldwide - US Nationwide distribution including in the states of AL, AZ, CA,…Official notice →- 2025-11-19
US
Becton Dickinson & Co. recalls BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution in the states of CO, CT, KY, NJ, TN,…Official notice →- 2025-10-29
US
Becton Dickinson & Co. recalls BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2.…
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of…
FDA · DeviceBecton Dickinson & Co.Worldwide distribution. US Nationwide including Guam and Puerto Rico, Algeria,…Official notice →- 2025-07-02
US
Becton Dickinson & Co. recalls BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to…
BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates.
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of AR, AU, BD, BE,…Official notice →- 2025-03-12
US
Becton Dickinson & Co. recalls BD BBL TB Stain Kit K, Catalog (REF): 212522
One component of the kit was shipped with an expiration date of 30Sep2024 while the Certificate of Analysis (COA) indicated an expiration date of 30Apr2025.
FDA · DeviceBecton Dickinson & Co.Domestic: AZ, CA, CO, GA, KY, IL, IN, NC, NJ, NY, MA, MD, TX, WA.…Official notice →- 2025-01-29
US
Becton Dickinson & Co. recalls BD PCR Cartridges used with MAX System. Model Number: 437519
Potential for signal drift in specific lots of BD PCR Cartridges.
FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →
Other drugs & medical recalls in the United States
- 2025-07-30
US
Medtronic, Inc. recalls Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application,…
In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's…
US
CooperVision, Inc. recalls Biofinity XR Toric Contact Lens
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
FDA · DeviceCooperVision, Inc.Worldwide distribution - US Nationwide and the countries of Brazil, Canada,…Official notice →US
Johnson & Johnson Vision Care, Inc. recalls ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Due to defects (bubbles/voids) identified during standard finished goods testing
FDA · DeviceJohnson & Johnson Vision Care, Inc.Worldwide - U.S. Nationwide distribution including in the states of AL, AZ,…Official notice →US
Bridge to Life Ltd recalls Bridge to Life EasiSlush, (Sodium Chloride Solution for Sterile Slush Preparation) (0.9% Sodium Chloride Irrigation, USP), Part Number REF…
The firm issued a field safety notice after becoming aware of three lots of products not having quarterly dose audits being completed on time in the first quarter of 2024. Routine lot by lot testing was completed…
FDA · DeviceBridge to Life LtdUnited States - New York, Maryland, Alabama, North Carolina, South Carolina,…Official notice →US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B;…
Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistributed domestically to California, Florida, Pennsylvania, and Texas. No…Official notice →US
Beckman Coulter Inc. recalls Estrone RIA, REF: DSL8700. Estrone RIA is an IVD used for the quantitative measurement of estrone in human serum and plasma.
A specific lot of bovine serum albumin (BSA) used for manufacturing of coated tubes (CT) that are included in the Estrone RIA kit lots caused different affinity of manufactured coated tubes to patient samples, causing…
FDA · DeviceBeckman Coulter Inc.US: North Carolina OUS: Argentina, Austria, Belgium, Canada, France, Germany,…Official notice →