Becton Dickinson & Company recalls BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination…
Read the official notice →- Date
- 2022-07-27
- Country
- United States
- Brand
- Becton Dickinson &
- Product
- BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide distribution in the states of AK, AR,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-11-23
USBecton Dickinson & Co. recalls BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most aerobic and facultative…
Misformulated minocycline-can cause erroneously increased Minimal Inhibitory Concentration (MIC) values when performing antibiotic susceptibility testing (AST) against minocycline and result in the reporting of false…
- 2022-10-26
- US
Becton Dickinson & Company recalls BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting,…
The affected product contains isobutylene which has recently demonstrated potential interference in determination of methanol by gas chromatography methods. The interference may lead to false positive results in…
FDA · DeviceBecton Dickinson & CompanyDistribution US nationwide, Canada, New Zealand, and Hong Kong.Official notice → - 2022-08-24
- US
Becton Dickinson & Company recalls BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the…
Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
FDA · DeviceBecton Dickinson & CompanyUS Nationwide Distribution CA FL GA IL MD MI OR PA PR TN TXOfficial notice → - 2022-05-11
- US
Becton Dickinson & Co. recalls BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10
When updating BD Kiestra customers to BD Synapsys version 4.10, the custom antibiotic codes set by the customer are overwritten with the BD default antibiotic codes.
FDA · DeviceBecton Dickinson & Co.Worldwide distribution US Nationwide distribution in the states of CA, IL, MI,…Official notice → - 2022-03-02
- US
Becton Dickinson & Company recalls BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port…
May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i or UX-2000 Analyzers and lead to false elevations in RBC counts
FDA · DeviceBecton Dickinson & CompanyUS Nationwide distribution in the state of IL.Official notice → - 2022-02-16
- US
Becton Dickinson & Co. recalls BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalog Number: 256066
May have the potential to overheat and/or cause fire, the issue can occur when an unauthorized alternative AC power adapter, and not the one provided by BD is used to power the instrument.
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of Armenia,…Official notice →
Other drugs & medical recalls in the United States
- 2022-07-27
- US
LumiraDx recalls LumiraDx SARS-CoV-2 Antibody (Ab) Liquid Quality Control
Modification to the LumiraDx SARS-CoV-2 Antibody (Ab) test that was made outside the scope of the approved EUA.
FDA · DeviceLumiraDxDomestic: AR, CA, FL, MA, MD, NC, NJ, NV, NY, OK, TN, TX, & WI.Official notice → - US
Aesculap Implant Systems LLC recalls Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 pieces per shipping unit, product code…
Packaging seal integrity not validated resulting in a lack of sterility assurance.
FDA · DeviceAesculap Implant Systems LLCUnited States: CA, CO, GA, IL, IN, KY, MI, NC, NE, NY, OH, RI, VA and WIOfficial notice → - US
Aesculap Implant Systems LLC recalls AESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code SWT113T. Used in spinal fusion surgery.
Insufficient clamping force of the cross connectors in the spinal surgical system which may lead to movement of the connectors on the rods and/or microparticle abrasion.
FDA · DeviceAesculap Implant Systems LLCUnited States Nationwide distribution in the states of CA, CO, IL, IN, MI, NC,…Official notice → - US
GE Healthcare, LLC recalls SIGNA Premier magnetic resonance scanner, model 5748519.
Under rare conditions, SIGNA Premier gradient coils could result in elevated acoustic noise during scanning. After prolonged periods of elevated acoustic noise, this could potentially lead to hearing loss.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice → - US
Aesculap Implant Systems LLC recalls ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Fracture or breakage of the spinal fixation arm at the downtube instrument if the 90 degree angle is not met when using the removal key with the spinal fixation system.
FDA · DeviceAesculap Implant Systems LLCUnited States Nationwide distribution in the states of CA, CO, IL, MI, OH & TX.Official notice → - US
GE Healthcare, LLC recalls GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.
The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls on a person.
FDA · DeviceGE Healthcare, LLCDistribution was made to AZ, CA, CO, CT, FL, IA, ID, IL, IN, KY, LA, MA, MD,…Official notice →