Manufacturer

Carefusion 2200 Inc

80 recalls in our database name Carefusion 2200 Inc as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

51–75 of 80

ModerateFDA (Devices)·Z-0389-2023·2022-12-14
Carefusion Bipolar Surgical Forceps Recalled for Missing Instructions
Carefusion 2200 Inc. is recalling 41 units of Hardy Bayonet Irrigating Bipolar Forceps due to incomplete instructions for use. The supplied instructions lack content about device power supply interface and maintenance procedures.
Product
Carefusion V. Mueller HARDY BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED, 0.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-1335
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0417-2023·2022-12-14
CareFusion Bipolar Surgical Forceps Recalled for Incomplete Operating Instructions
CareFusion bipolar surgical forceps recalled for incomplete Instructions for Use. Documentation is missing information on power supply interface and cleaning procedures.
Product
CareFusion V. Mueller CUSHING MICRO BIPOLAR FORCEPS 0.7MM TIP, OVERALL LENGTH 6" (150MM), REF F-52000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0388-2023·2022-12-14
Bipolar Irrigating Forceps Recall: Missing Power Supply and Maintenance Instructions
Carefusion is recalling 132 units of V. Mueller bipolar irrigation forceps due to incomplete instruction manuals missing power supply interface and maintenance guidance.
Product
Carefusion V. Mueller SCOVILLE-GREENWOOD BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED, 1.5MM TIP OVERALL LENGTH 7-3/4" (195MM), REF F-1305
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0381-2023·2022-12-14
Bipolar forceps recalled for incomplete instructions for use
Carefusion recalled certain bipolar forceps due to incomplete Instructions For Use. The IFU was missing content about the device's power supply interface and cleaning and maintenance procedures.
Product
Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, OVERALL LENGTH 7-1/2" (190MM), REF F-1111
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0391-2023·2022-12-14
Surgical Bipolar Forceps Recalled for Incomplete Operating Instructions
Carefusion is recalling bipolar surgical forceps due to incomplete Instructions for Use. The missing instructions cover power supply interface and cleaning procedures.
Product
Carefusion V. Mueller" CUSHING BAYONET BIPOLAR FORCEPS, 2.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-2004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0383-2023·2022-12-14
Bipolar Forceps Recall Due to Incomplete Instructions for Use
Carefusion is recalling 259 surgical bipolar forceps units because the Instructions for Use are missing critical information about power supply interface and maintenance procedures.
Product
Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-1113
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0403-2023·2022-12-14
CareFusion Bipolar Forceps Recalled: Incomplete Instructions for Power Supply
CareFusion is recalling bipolar forceps units due to incomplete instructions for power supply interface and device maintenance. The recall affects devices distributed worldwide.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5022
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0396-2023·2022-12-14
CareFusion Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar forceps are recalled due to incomplete manufacturer instructions for use. Missing content covers power supply interface and device maintenance and cleaning procedures.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5002
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0412-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Missing Instruction Manual Content
CareFusion bipolar forceps recalled due to missing instructions on power supply interface and cleaning/maintenance procedures. Corrected documentation is now available.
Product
CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT, 0.25MM TIP OVERALL LENGTH 6" (150MM) , REF F-5128
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0414-2023·2022-12-14
CareFusion Bipolar Surgical Forceps Recalled for Incomplete Instructions
CareFusion bipolar surgical forceps are being recalled because their instruction manual is missing critical information about power supply interface and cleaning procedures. BD is providing corrected instructions to healthcare facilities.
Product
CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED STRAIGHT FINE, 0.5MM TIP OVERALL LENGTH 8-3/4" (225MM), REF F-5302
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0406-2023·2022-12-14
Bipolar Forceps Recall: Missing Instructions for Power Supply and Maintenance
CareFusion bipolar forceps are being recalled due to missing Instructions for Use content about power supply interface, cleaning, and maintenance. Users should obtain the complete manufacturer instructions immediately.
Product
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5069
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0402-2023·2022-12-14
Medical Device Recall: Missing Instructions for Bipolar Surgical Forceps
CareFusion bipolar forceps recalled because the provided instructions are missing critical information about power supply interface and cleaning procedures. No injuries reported.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS,1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5018
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2023·2022-11-23
CareFusion sterilization containers fail aerosol challenge testing
CareFusion GENESIS sterilization containers have not consistently met aerosol challenge testing requirements. The FDA is recalling 510 units to prevent potential sterilization failures.
Product
CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD2-5ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0215-2023·2022-11-23
GENESIS Full-Length Sterilization Containers recalled for failed aerosol testing
CareFusion 2200 Inc recalls GENESIS sterilization containers (model CD3-7ST, all lots) that have not consistently met aerosol challenge testing requirements required for proper sterilization efficacy.
Product
CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD3-7ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0218-2023·2022-11-23
CareFusion GENESIS Sterilization Containers Recalled for Inadequate Aerosol Challenge Testing
Carefusion 2200 Inc is recalling 562 Genesis STERRAD reusable sterilization containers due to failure to consistently meet aerosol challenge testing requirements, used to sterilize surgical instruments in healthcare facilities.
Product
CareFusion V.Mueller GENESIS LARGE, SHALLOW CONT. 28 X 11" (71.1 X 27.9CM) 3" (7.6CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-3ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0212-2023·2022-11-23
CareFusion Genesis Sterile Containers Recalled for Failed Sterilization Validation Testing
CareFusion is recalling 308 units of Genesis sterilization containers that failed aerosol challenge testing required to ensure proper sterilization of surgical instruments. The containers were distributed in the US and multiple countries.
Product
CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0219-2023·2022-11-23
CareFusion Genesis sterilization containers fail aerosol challenge test requirements
CareFusion Genesis reusable sterilization containers have not consistently passed aerosol challenge testing, which verifies their ability to properly sterilize medical instruments. Approximately 537 units were distributed internationally.
Product
CareFusion V.Mueller GENESIS LARGE, CONTAINER 28 X 11" (71.1 X 27.9CM) 6" (15.2CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-61ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0211-2023·2022-11-23
CareFusion sterile containers fail aerosol sterilization test requirement
CareFusion GENESIS sterilization containers did not consistently meet aerosol challenge testing requirements. These containers are used in healthcare facilities to sterilize surgical instruments.
Product
CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 8" (20.3CM) DEEP STERRAD COMPATIBLE, REF CD2-8ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0205-2023·2022-11-23
CareFusion Genesis STERRAD containers fail sterilization testing
Healthcare sterilization containers failed aerosol challenge testing, indicating potential inadequate sterilization of surgical instruments. 493 units affected across US and international markets.
Product
CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD1-4ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0208-2023·2022-11-23
CareFusion GENESIS Sterilization Containers Fail Aerosol Validation Testing
CareFusion V.Mueller GENESIS sterilization containers have not consistently met aerosol challenge testing requirements. The recall affects 319 units distributed in the US and internationally.
Product
CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD2-4ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0206-2023·2022-11-23
CareFusion GENESIS Sterilization Containers Fail Aerosol Challenge Testing
CareFusion GENESIS sterilization containers have not consistently met aerosol challenge testing requirements. Approximately 1,132 units distributed to healthcare facilities in the U.S. and internationally are affected.
Product
CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD1-5ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0203-2023·2022-11-23
CareFusion Genesis Mini Sterilization Containers fail aerosol testing
CareFusion Genesis Mini Containers used for surgical instrument sterilization have not consistently met aerosol challenge testing requirements, which may affect their ability to protect instruments during sterilization.
Product
CareFusion V.Mueller GENESIS MINI CONTAINER 10-1/2 X 7-1/2" (26.7X19.0CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF CD0-3ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0214-2023·2022-11-23
CareFusion Genesis Sterilization Containers Fail Aerosol Challenge Testing
CareFusion Genesis sterilization containers have failed to consistently meet aerosol challenge testing, potentially leaving surgical instruments inadequately sterilized. 318 units distributed in the US and internationally.
Product
CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0210-2023·2022-11-23
CareFusion Genesis sterilization containers recalled for failed sterility testing
CareFusion Genesis reusable sterilization containers are recalled after failing aerosol challenge testing requirements. No illnesses or injuries have been reported.
Product
CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD2-6ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0204-2023·2022-11-23
CareFusion Sterilization Containers Fail Aerosol Challenge Testing
CareFusion Genesis sterilization containers failed required aerosol challenge testing. The 1,143 affected units may not adequately sterilize surgical instruments.
Product
CareFusion V.Mueller GENESIS QTR-LENGTH CONTAINER 12 X 8" (30.3X20.3CM) 4" (10.2CM) DEEP STERRAD COMPATIBLE, REF CD0-4ST
Category
Medical Device
Distribution
0 states