Reported Dec 11, 2024 · Ongoing
BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988
Becton Dickinson & Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212
Is this the product you have?
- BD COR PX Instrument Version or Model443988
- Catalog Number443988
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 443988— — 00382904439880UDI-DI: 00382904439880 — Serial Numbers: CRP0007, CRP0025, CRP0045, CRP0064, CRP0058, CRP0060, CRP0055, CRP0040, CRP0056, CRP0038, CRP0057, CRP0062, CRP0046, CRP0031, CRP0068, CRP0053, CRP0034, CRP0041, CRP0021, CRP0054, CRP0004, CRP0001, CRP0008, CRP0009, CRP0012, CRP0013, CRP0014, CRP0017, CRP0018, CRP0048, CRP0051, CRP0027, CRP0042, CRP0069, CRP0074, CRP0032, CRP0075, CRP0077, CRP0080, CRP0079, CRP0024, CRP0011, CRP0010, CRP0016, CRP0019, CRP0028, CRP0061, CRP0063, CRP0033, CRP0044, CRP0066, CRP0067, CRP0071, CRP0043, CRP0003, CRP0026, CRP0036, CRP0050, CRP0049, CRP0070, CRP0065, CRP0059, VSP0010, CRP0052, CRP0073, CRP0072 - Amount recalled
- 66 units (18 US, 48 OUS)
This recall covers 14 products
The agency filed one notice per product. You are reading one of them; the other 13 are below.
1 more are in the archive.
Where it was sold
Why it was recalled
BD confirmed that 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 unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
This product could cause temporary or reversible health problems — stop using it.
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