CareFusion 303, Inc. recalls BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 .…
The automated dispensing cabinet software update included a .dll file that is not compatible with MedBank Cabinet stations with MedCart Matrix drawers. The cabinet system will stop functioning (Matrix drawers will stop…
Read the official notice →- Date
- 2022-10-05
- Country
- United States
- Brand
- CareFusion
- Product
- BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 .…
- Classification
- Class II
- Units
- U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 CareFusion recalls
- 2023-01-18
USCareFusion 303, Inc. recalls BD Pyxis MedBank System - Product Label/labeling pending
Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result…
FDA · DeviceCareFusion 303, Inc.U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CO,…Official notice →- 2022-12-14
- US
Carefusion 2200 Inc recalls CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2" (240MM) , REF F-5008
XXX
FDA · DeviceCarefusion 2200 IncNationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines,…Official notice → - US
Carefusion 2200 Inc recalls Carefusion V. Mueller" CUSHING BAYONET BIPOLAR FORCEPS, 2.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-2004
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface with the device power…
FDA · DeviceCarefusion 2200 IncNationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines,…Official notice → - 2022-11-23
- US
Carefusion 2200 Inc recalls CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
FDA · DeviceCarefusion 2200 IncUS and Australia, Bahrain, Canada, Denmark, Hong Kong, Italy, Japan, Malaysia,…Official notice → - 2022-09-28
- US
CAREFUSION recalls BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock, REF: MX4436
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may…
FDA · DeviceCAREFUSIONUS: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC,…Official notice → - 2022-04-06
- US
Carefusion 2200 Inc recalls (a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b) CareFusion…
The finished device package did not contain the IFU.
FDA · DeviceCarefusion 2200 IncWorldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice →
Other drugs & medical recalls in the United States
- 2022-10-05
- US
Unomedical A/S recalls Autosoft 90, model numbers 1000282, 1002817, 1002818, 1002819, 1002820, 1002821, 1002822, 1002823, and 1002824. Infusion sets used with…
The IFU incorrectly states the insulin fill value of two sizes of cannula which can result in an initial insulin infusion to be fewer units than intended.
FDA · DeviceUnomedical A/SDistribution was made to California. There was no government/military…Official notice → - US
Mckesson Medical-Surgical Inc. Corporate Office recalls SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll Ethylene Oxide (EO) Gas / Steam 3 Inch X…
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
FDA · DeviceMckesson Medical-Surgical Inc. Corporate OfficeUS Nationwide distribution.Official notice → - US
Micro-X Ltd. recalls MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19
Software calibration error with product equip with a Dose Area Product (DAP) meter. This results in the product displaying the incorrect DAP meter values which may impede radiation exposure management decisions
FDA · DeviceMicro-X Ltd.Worldwide distribution - U.S. Nationwide distribution in the states of CA, NV,…Official notice → - US
SunMed Holdings, LLC recalls Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH, REF Number 3373-91
The kits are being recalled due to a lack of sterility of a spare needle contained within the kits. There is a potential for skin infection or sepsis if the patient is exposed to a non-sterilized, unused needle.
FDA · DeviceSunMed Holdings, LLCDomestic distribution to AL, FL, GA, IL, LA, MO, NJ, NY, TN, TX.Official notice → - US
Howmedica Osteonics Corp. recalls Short tibial bearing MK4 - Std, STM, Catalog No. SMMLTB02. Knee prosthesis component.
A MK4 Tibial Bearing was supplied with the intention to mate with the Tibial Metal Casing in-situ. However, the device in-situ was a MK3 Tibial Metal Casing. The supplied MK4 tibial bearing was not exchangeable for the…
FDA · DeviceHowmedica Osteonics Corp.Distributed to one customer located in New York.Official notice → - US
Collagen Matrix Inc recalls Collagen Dental Wound Dressing - Bovine Dermis Tap, 25mm x 75mm Product was distributed under the following brand names: 1) Cytoplast…
The packaging may not be sealed, which could compromise sterility.
FDA · DeviceCollagen Matrix IncUS distribution to distributors in IL, IN, MI, NC, OH, and TXOfficial notice →