State

Kansas product recalls

73,817 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,053
Severe: 1,486
Most recent: 2026-11-04

Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47751–47775 of 79639

HighFDA (Drugs)·D-0543-2017·2017-03-22
Synergy Rx Recalls Salicylic Acid and 5-FU Products for Sterility Concerns
Synergy Rx is recalling salicylic acid and 5-FU prescription products due to lack of assurance of sterility and CGMP deviations.
Product
SALICYLIC ACID SOLUTION in all strengths including 20%, 25%, 30%, and 40%, SALICYCLIC ACID 20%. 2.5%5-FU, SALICYCLIC ACID 20%, 5-FU 2.5% CREAM, SALICYCLIC ACID 20%/5-FU 2.5% MEDICATION STICK, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1447-2017·2017-03-22
LeMaitre Vascular Catheter Recalled for Missing Latex Warning Symbol
LeMaitre Vascular is recalling Reddick Scoop Tip Cholangiogram Stiffer Catheters because the latex warning symbol was missing from the packaging.
Product
LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper IFU) REF# 2401-50
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1461-2017·2017-03-22
Kiscomedica Recalls L-Varlock Cage/Trial Implant Holder Due to Breakage
Kiscomedica S.A. is recalling 13 units of the L-Varlock Cage/Trial Implant Holder because the tip holder broke during use.
Product
L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for intervertebral body fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the lumbar spine at one…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0588-2017·2017-03-22
Synergy Rx Recalls Tretinoin Cream and Gel Due to Sterility Concerns
Synergy Rx is recalling Tretinoin Cream and Gel in all strengths due to a lack of assurance of sterility and CGMP deviations.
Product
TRETINOIN CREAM in all strengths including: 0.1%, 0.05%, TRETINOIN GEL in all strengths including 0.1% and 0.05%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1607-2017·2017-03-22
Choice Farms Stuffed Mushrooms Recalled for Listeria Contamination
Del Monte Fresh Produce is recalling Choice Farms Stuffed Mushrooms due to possible Listeria monocytogenes contamination. The product was distributed in Texas and Kansas.
Product
CHOICE FARMS Stuffed Mushrooms, 7 oz. INDIVIDUAL SHRINK-WRAPPED TRAYS
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1397-2017·2017-03-22
Toshiba Kalare X-ray Generator Recalled for Premature Exposure Termination
Toshiba American Medical Systems Inc is recalling 254 Kalare DREX-KL80 X-ray generators because the system may terminate exposure prematurely during an examination.
Product
Toshiba Kalare DREX-KL80 X-ray generator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2017·2017-03-22
Medtronic Recalls BNX Fine Needle Aspiration Systems Due to Breakage Risk
Medtronic is recalling 1,096 units of BNX Fine Needle Aspiration Systems because the handle may break during use.
Product
BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01
Category
Medical Device
Distribution
40 states
ModerateFDA (Devices)·Z-1480-2017·2017-03-22
Philips BrightView Nuclear Imaging Systems Recalled for Motion and Software Issues
Philips Medical Systems is recalling 1,218 BrightView nuclear imaging systems worldwide due to four issues, including motion controller failures and software freezes.
Product
882480: BrightView designed for single or dual detector nuclear imaging accommodating a range of ECT studies. In addition it can be used to perform planar static, dynamic, gated, total body, circular-orbit and noncircular orbit SPECT, gated SPECT (circular and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1444-2017·2017-03-22
LeMaitre Vascular Cholangiogram Catheter Recalled for Missing Latex Symbol
LeMaitre Vascular is recalling 608 Reddick Cholangiogram Catheters because the latex warning symbol was not printed on the packaging.
Product
LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF # e2400-52
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1466-2017·2017-03-22
Siemens Artis Q and Q.Zen Fluoroscopic X-Ray System Recall
Siemens is recalling Artis Q and Q.Zen fluoroscopic x-ray systems because a gap in the wireless foot switch housing could allow liquids to penetrate the interior, potentially causing the switch to fail.
Product
Artis Q and Q.Zen fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1451-2017·2017-03-22
LeMaitre Vascular Cholangiogram Catheter Recalled for Missing Latex Symbol
LeMaitre Vascular is recalling 247 units of Scoop Tip Cholangiogram Catheters because the latex warning symbol was missing from the packaging.
Product
LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper IFU) REF# 2401-52
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1458-2017·2017-03-22
Terumo Level Sensor II Pads Recalled for Non-Compliant Expiration Date Labeling
Terumo Cardiovascular Systems Corporation is voluntarily recalling Level Sensor II Pads because the expiration date format may not be recognizable to all users.
Product
Terumo Advanced Perfusion System 1-Level Sensor II Pads, Product Usage: Ultrasonic couplant used to facilitate the transmission of sound energy between the level sensor and the reservoir.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0542-2017·2017-03-22
Synergy Rx Recalls Retinoic Acid Solution Due to Sterility Concerns
Synergy Rx is recalling all lots of Retinoic Acid Solution due to a lack of assurance of sterility and CGMP deviations.
Product
RETINOIC ACID SOLUTION in all strengths including 0.3%, 0.4%, 0.5%, 1%, RETINOIC ACID SOLUTION LIQUID, 0.4%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0592-2017·2017-03-22
Synergy Rx Recalls RETIN-A 0.05% Cream Due to Sterility Concerns
Synergy Rx is recalling RETIN-A 0.05% Cream because of a lack of assurance of sterility and CGMP deviations.
Product
RETIN-A 0.05% CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1459-2017·2017-03-22
Terumo Level Sensor Gel Pads Recalled for Non-Compliant Labeling
Terumo is voluntarily recalling Level Sensor II Gel Pads because the expiration date format may not be recognizable to all users.
Product
Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Usage: Level sensor pads are used to attach the level sensors to a hard shell reservoir. includes coupling gel.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0595-2017·2017-03-22
Synergy Rx Recalls Metronidazole and Azelaic Acid Products for Sterility Concerns
Synergy Rx is recalling Metronidazole 1% Gel and Metronidazole/Niacinamide/Azelaic Cream due to lack of assurance of sterility and CGMP deviations.
Product
METRONIDAZOLE 1% GEL, METRONIDAZOLE 1%/ NIACINAMIDE 4%/ AZELAIC CREAM 10% CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1457-2017·2017-03-22
Merge Hemo software recalled due to study tab locking issue
Merge Healthcare is recalling Merge Hemo software versions 6.10 through 9.40.3 because the system may incorrectly lock study tabs, potentially preventing access to data.
Product
Merge Hemo software. Product Usage: Merge Hemo is a hemodynamic monitoring system that records and displays physiological data.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1450-2017·2017-03-22
LeMaitre Vascular Scoop Tip Cholangiogram Catheter Recalled for Missing Latex Symbol
LeMaitre Vascular is recalling 4,673 units of Scoop Tip Cholangiogram Catheters because the latex warning symbol was not printed on the packaging.
Product
LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-52
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0538-2017·2017-03-22
Synergy Rx Fluocinonide Solution Recalled for Sterility Assurance Issues
Synergy Rx is recalling Fluocinonide 0.05% Solution due to a lack of assurance of sterility and CGMP deviations.
Product
FLUOCINONIDE 0.05% SOLUTION, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0532-2017·2017-03-22
Synergy Rx Recalls Betamethasone Creams and Ointments for Sterility Concerns
Synergy Rx is recalling various betamethasone cream and ointment products due to a lack of assurance of sterility and CGMP deviations.
Product
BL 20%/4% CREAM, BLT 20%/6%/4% CREAM, BLT 20%/6%/6%, BLT 20% 8% 4% CREAM, BLT 20% 8% 4% OINTMENT, BLT 20% 8% 6% CREAM, BLT 20%/ 8% /8% OINTMENT, BLT 20%/ 8% /8% CREAM, BLT 20%/ 7%/ 7% CREAM, BLT 20%/ 10%/ 4% CREAM, BLT 20%/ 10%/ 10% CREAM, BLT 20%/ 20%/ 10% OINTMENT,BLT 7%…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0582-2017·2017-03-22
Synergy Rx Enhanced Retin Cream Recalled for Sterility Assurance Issues
Synergy Rx is recalling Enhanced Retin Anti-Wrinkle Cream due to lack of assurance of sterility and CGMP deviations.
Product
ENHANCED RETIN ANTI-WRINKLE CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1463-2017·2017-03-22
Radiometer ABL800 Blood Gas Analyzer Recall for Sample Type Change
Radiometer America Inc. is recalling ABL800 analyzers because the 'cord blood' sample type was changed to 'cord blood arterial' and 'cord blood venous.'
Product
The ABL800 Model#:All
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1445-2017·2017-03-22
LeMaitre Vascular Cholangiogram Catheter Recalled for Missing Latex Labeling
LeMaitre Vascular is recalling 250 units of Reddick Cholangiogram Stiffer Catheters because the latex warning symbol was not printed on the packaging.
Product
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0558-2017·2017-03-22
Synergy Rx Recalls Generic VI Peel Due to Sterility Concerns
Synergy Rx is recalling Generic VI Peel products nationwide due to a lack of assurance of sterility and CGMP deviations.
Product
GENERIC VI PEEL (Sal Acid 2%, TCA 7% Phenol 7%, Retinoic Acid 0.4%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1467-2017·2017-03-22
Siemens Artis Zee and Zeego Fluoroscopic X-Ray System Recall
Siemens is recalling Artis Zee and Zeego fluoroscopic x-ray systems because a gap in the wireless foot switch housing could allow liquids to penetrate the interior, potentially causing the switch to fail.
Product
Artis Zee and Zeego fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide