Manufacturer

WalkMed Infusion, LLC

19 recalls in our database name WalkMed Infusion, LLC as the manufacturing or recalling firm.

What the numbers show

Total: 19
Critical: 0
Severe: 0
Most recent: 2016-07-27

Of the 19 recalls from WalkMed Infusion, LLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

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.

1–19 of 19

HighFDA (Devices)·Z-2229-2016·2016-07-27
WalkMed Infusion Recalls IV Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling T100-000F IV sets due to the potential presence of particulate matter in or on the devices.
Product
T100-000F, 100" IV Set with Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2219-2016·2016-07-27
WalkMed Infusion Pumps Recalled for Unapproved Software and Specification Changes
WalkMed Infusion is voluntarily recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.
Product
The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2226-2016·2016-07-27
WalkMed Recalls IV Administration Sets Due to Potential Particulate Presence
WalkMed Infusion, LLC is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T090-022V 90" 20 Drop IV Admin Set Needle free Y-Site & 0.22 Fltr. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2224-2016·2016-07-27
WalkMed Recalls IV Administration Sets Due to Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T090-000V 90" 20 Drop IV Admin Set w/ Needlefree Y-Site. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2223-2016·2016-07-27
WalkMed Recalls IV Administration Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2222-2016·2016-07-27
WalkMed Recalls IV Administration Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2235-2016·2016-07-27
WalkMed Recalls IV Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T100-022WF, IV Set with 2 Y-Sites, 0.22 micron filter, Back Check Valve, & FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2231-2016·2016-07-27
WalkMed Recalls IV Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T100-000WF, IV Set with Upper Y-Site, Lower Y-Site, Back Check Valve, and Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2230-2016·2016-07-27
WalkMed Recalls IV Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of T100-000VF IV sets due to the potential presence of particulate matter in or on the devices.
Product
T100-000VF, IV Set with Lower Y Site and Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2227-2016·2016-07-27
WalkMed Recalls IV Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of IV sets with 0.22 micron filters due to the potential presence of particulate matter in or on the devices.
Product
T095-022, IV Set with 0.22 Micron Filter. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2228-2016·2016-07-27
WalkMed Recalls IV Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of IV administration sets due to the potential presence of particulate matter on or in the devices.
Product
T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2234-2016·2016-07-27
WalkMed Infusion Recalls IV Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T105-000WC IV Set w/2 Y-Sites, BC Vlv & Filter Cap. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2232-2016·2016-07-27
WalkMed Infusion Recalls Triton Administration Sets Due to Particulate Presence
WalkMed Infusion is voluntarily recalling Triton Administration Sets because they may contain particulate matter. The recall affects 383 cases distributed nationwide.
Product
T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2233-2016·2016-07-27
WalkMed Infusion Recalls Triton Administration Sets Due to Particulate Presence
WalkMed Infusion is voluntarily recalling Triton Administration Sets due to the potential presence of particulate matter in or on the devices.
Product
T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2221-2016·2016-07-27
WalkMed Infusion Recalls Spike Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling 12-inch Microbore Spike Sets due to the potential presence of particulate matter in or on the devices.
Product
Spike Set, 12" Microbore SPM-12. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2225-2016·2016-07-27
WalkMed Recalls IV Administration Sets Due to Potential Particulate Presence
WalkMed Infusion is voluntarily recalling specific IV administration sets due to the potential presence of particulate matter in or on the devices.
Product
T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Back Check Valve. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2220-2016·2016-07-27
WalkMed Infusion Pumps Recalled for Unapproved Software and Specification Changes
WalkMed Infusion is recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.
Product
The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0242-2016·2015-11-18
WalkMed Infusion Pumps Recalled for Air Detection Failure
WalkMed Infusion is recalling Triton Infusion Pumps because they may fail to detect air in the line when infusing Venofer.
Product
Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volumetric Infusion Pump). Used to pump fluids into a patient in a controlled manner.
Category
Medical Device
Distribution
22 states
ModerateFDA (Devices)·Z-1122-2014·2014-03-12
WalkMed Recalls Triton FP Infusion Pumps Due to Labeling Error
WalkMed Infusion is recalling 797 Triton FP Infusion Pumps because the label on the right side contains an incorrect instruction.
Product
Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for delivering infusions of medications, as well as providing TPN (Total Parenteral Nutrition) and PCA (Patient Control Analgesia). It is intended for use in hospit
Category
Medical Device
Distribution
3 states