Becton, Dickinson and Company, BD Biosciences recalls BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF:…
Multitest with compromised raw material used to assess immune system status may result in flow cytometry plot with unusual staining pattern, nonspecific aggregates, high background, double positive event increase on…
Read the official notice →- Date
- 2024-07-24
- Country
- United States
- Brand
- Becton, Dickinson and Company, BD Biosciences
- Product
- BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF: 337166; BD Multitest…
- Classification
- Class II
- Units
- US: MN, NJ, NY, MD, UT, FL, NC, MA, KY, NE, NV, CA, LA, DC, OH, MI, PA, WA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 and Company, BD Biosciences recalls
- 2024-01-17
USBecton, Dickinson and Company, BD Biosciences recalls CD11b APC: ASR, REF: 340936, and CE, REF: 333143
In vitro diagnostics product that impacts the quality of cell staining can cause low or dim fluorescence signal, which can lead to potential false negative results and misdiagnosis of hematological malignancy, delayed…
FDA · DeviceBecton, Dickinson and Company, BD BiosciencesWorldwide - US Nationwide distribution including in the states of IL, MN, FL,…Official notice →- 2022-11-09
- US
Becton, Dickinson and Company, BD Biosciences recalls BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995), for use with BD FACSLyric, BD…
Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant.
FDA · DeviceBecton, Dickinson and Company, BD BiosciencesU.S.: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA,…Official notice → - 2022-06-08
- US
Becton, Dickinson and Company, BD Biosciences recalls BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific reagent for the Anti-Kappa antibody, which specifically…
Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic flow profiles.
FDA · DeviceBecton, Dickinson and Company, BD BiosciencesWorldwide distribution - US Nationwide distribution in the states of AL, CA,…Official notice →
Other drugs & medical recalls in the United States
- 2024-07-24
- US
Medical Depot Inc. recalls Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily…
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
- US
Qiagen Sciences LLC recalls QIAcube Connect MDx - IVD Instrument designed to perform automated isolation and purification of nucleic acids in molecular diagnostic…
Heater shaker module does not perform heating if the temperature is set below 40¿C for static incubation steps when running IVD protocol QIAamp¿ DSP DNA Mini Kit (cat. no. 61304), Protocol: Isolation of genomic DNA…
FDA · DeviceQiagen Sciences LLCNationwide. Foreign: AD, AT, AU, BE, CA, CH, CN, CZ, DE, DK, ES, FI, FR, GB,…Official notice → - US
Medtronic Neuromodulation recalls Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (catheter pump revision kit)
Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and 8784. The intent of the design update is to reduce the potential for tissue growth into the Ascenda catheter connector which may potentially lead…
FDA · DeviceMedtronic NeuromodulationWorldwide Distribution: US (nationwide) and OUS (foreign) countries of:…Official notice → - US
Boston Scientific Corporation recalls Autotome RX 20mm CUT WIRE Cannulating Sphincterotome, Material Number (UPN) M00545170. The device is used in selective cannulation…
Foreign material may be present on the enclosed section of the cutting wire which may lead to inability to optimally bow the sphincterotome. This issue may lead to prolongation of procedure.
- US
Cadwell Industries Inc recalls Cascade IOMAX Cortical Module, REF: 190296-200
Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.
FDA · DeviceCadwell Industries IncUS: IL CA OUS: Canada, Germany, India, Italy, Mexico, Poland, South Africa,…Official notice → - US
St. Jude Medical recalls St. Jude Medical Agilis NxT Steerable Introducer, REF 408309
One lot of product has dilators that are too short and will not extend outside the introducer sheath.