State

Nevada product recalls

72,907 recalls have nationwide distribution and so reach Nevada. 5,692 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total: 5,692
Critical: 951
Severe: 1,476
Most recent: 2026-09-09

Of the 5,692 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,476 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,692 recalls whose distribution notice names Nevada specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1151–1175 of 78599

SevereFDA (Devices)·Z-2369-2026·2026-06-24
Arrow antimicrobial PSI kits contain drugs from a recalled supplier
Arrow PSI and PSI/CVC kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 348,684 units are affected.
Product
Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU4; PSI/CVC KIT: 9 FR/7 FR X 6IN (16CM)/ASK-09903-AMC1; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-CMC1; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU4; PSI KIT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2374-2026·2026-06-24
Arrow AHDC catheter kits contain drugs from a recalled supplier
Arrow AHDC three-lumen catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 4,270 units affected.
Product
Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XP1A; AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XP1A; AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPN1A; AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2392-2026·2026-06-24
Arrow access tray MC3 contains drugs from a recalled supplier
The Arrow Access Tray, REF ASK-04001-MC3, is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 8,265 units affected.
Product
Description/REF: ACCESS TRAY/ASK-04001-MC3
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2370-2026·2026-06-24
Arrow PICC and Delta kits contain drugs from recalled supplier
Arrow PICC and PICC/Delta kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 37,738 units are affected.
Product
Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA PICC/DELTA: 2L 5.5 FR X 50 CM/ASK-45052-NS AGBA PICC/DELTA KIT: 1L 4.5 FR X 55 CM/ASK-45541-MHBV PICC KIT: 2L 5.5 FR X 55 CM CG+ VPS/ASK-45552-RH AGBA PICC NaviCurve: 2L 5.5FR x 55CM BP/DLX-45552-CURV
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2395-2026·2026-06-24
Arrow PICC access trays contain drugs from a recalled supplier
The Arrow PICC Access Tray, REF ASK-04001-CG1, is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 360 units affected.
Product
Description/REF: PICC ACCESS TRAY/ASK-04001-CG1
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V402000·2026-06-24
Ford Recalls 2018-2021 SUVs and 2021 F-150s for Transmission Defect
Ford is recalling specific 2018-2021 SUVs and 2021 F-150s because the transmission park pawl may engage while moving, risking vehicle rollaway and crashes.
Product
FORD — FORD, LINCOLN F-150, AVIATOR, EXPLORER, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2384-2026·2026-06-24
Arrow access trays and multilumen CVC kits contain recalled drugs
Arrow access trays and multilumen PI CVC kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 1,061,069 units affected.
Product
Description/REF: ACCESS TRAY/ASK-04001-JHH; ACCESS TRAY/ASK-04001-LMDTG; PI CVC KIT: 3 LUMEN 7 FR X 6 IN (16 CM)/ASK-12703-PSPH1; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-WMC2; MULTILUMEN PI CVC KIT: 3L 7 FR X 20CM/ASK-15703-LMDT1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20CM/ASK-15703-LMDTG1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2470-2026·2026-06-24
ConMed AirSeal 5mm 120mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 5 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 120 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2461-2026·2026-06-24
Stryker Triathlon size 3 baseplate packaging contained a size 4 implant
Triathlon Universal Baseplate Size 3 packaging is being recalled after Stryker identified that it contained a Size 4 baseplate, and vice versa. Seven units are affected.
Product
TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2487-2026·2026-06-24
Medline open heart and cardiac kits contain catheters failing specifications
Medline open heart and cardiac procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 168,968 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2501-2026·2026-06-24
Medline labour delivery and vaginal kits contain substandard catheters
Medline labour and delivery and vaginal procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 24,388 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK, Medline Kit Number/SKU DYNJ47625B; 2) GYN VAGINAL, Medline Kit Number/SKU DYNJ912219; 3) KIT MAJ VAG SET UP, Medline Kit Number/SKU DYNJ907033B; 4) MINOR VAG PACK, Medline Kit Number/SKU DYNJ68663B; 5) OB DELIV
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2518-2026·2026-06-24
HeartMate 3 assist system kits recalled over backup battery failures
HeartMate 3 Left Ventricular Assist System kits, model 106524US, are being recalled due to 11 volt backup battery failures. Four units are affected.
Product
Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a me
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2516-2026·2026-06-24
Inspire stimulation leads labeled with Use By dates beyond shelf life
Inspire Stimulation Leads, model 4063, are being recalled because they carry an incorrect Use By Date extending beyond the validated three-year shelf life. 10 units affected.
Product
Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire stimulation Lead Model/Catalog Number: 4063 Product Description: The Inspire¿ Stimulation Lead (Model 4063) is designed to deliver stimulation to the hypoglossal nerve for the treatment of obstructive sleep apnea.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2466-2026·2026-06-24
ConMed AirSeal 12mm blunt tip 100mm ports may trigger overpressure alerts
ConMed AirSeal 12 mm Access Ports and Obturators with Blunt Tip, 100 mm length, are being recalled because of the potential for overpressure alerts. 1,261 packs affected.
Product
ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2513-2026·2026-06-24
iLet Bionic Pancreas pumps may become stuck on the lock screen
The iLet Bionic Pancreas is being recalled because a screen unlock failure can leave the user stuck on the Lock Screen, unable to change the cartridge or announce a meal.
Product
iLet Bionic Pancreas, REF: BB1001
Category
Medical Device
Distribution
51 states
HighFDA (Devices)·Z-2515-2026·2026-06-24
Inspire respiratory sensing leads labeled with Use By dates beyond shelf life
Inspire Respiratory Sensing Leads, model 4340, are being recalled because they carry an incorrect Use By Date extending beyond the validated three-year shelf life. 50 units affected.
Product
Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire Respiratory Sensing Lead Model/Catalog Number: 4340 Software Version: N/A Product Description: The Inspire¿ Respiratory Sensing Lead (Model 4340) is designed to detect respiratory effort. The lead features a pres
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2471-2026·2026-06-24
ConMed AirSeal 5mm 100mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 5 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 100 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2494-2026·2026-06-24
Medline tonsil packs contain catheters failing performance specifications
Medline Tonsil Pack Cath procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 384 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: TONSIL PACK CATH, Medline Kit Number/SKU DYNJ65199A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2508-2026·2026-06-24
Medline CRANI procedure kits contain catheters failing performance specifications
Medline CRANI procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 3,521 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) CRANI, Medline Kit Number/SKU DYNJ908097; 2) CRANI, Medline Kit Number/SKU DYNJ908097A; 3) CRANI, Medline Kit Number/SKU DYNJ908097B; 4) CRANI, Medline Kit Number/SKU DYNJ908097C; 5) CRANI, Medline Kit Number/SKU DYNJ908097
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2476-2026·2026-06-24
Giraffe OmniBed Carestation canopy fasteners can fall into patient compartment
Giraffe OmniBed Carestations are being recalled because fasteners securing the canopy soffit can disengage and fall into the patient compartment. 23,430 units affected.
Product
Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant warmer, Model Numbers 2082844-001-XXX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2489-2026·2026-06-24
Medline vasectomy reversal kits contain catheters failing performance specifications
Medline Bilateral Micro Vasectomy Reversal kits are being recalled because representative samples did not meet applicable catheter performance specifications. 588 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL, Medline Kit Number/SKU DYNJ68302
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2490-2026·2026-06-24
Medline oral restoration kits contain catheters failing performance specifications
Medline Oral Restoration procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications.
Product
MEDLINE Medical Procedure Kits labeled as: ORAL RESTORATION, Medline Kit Number/SKUDYNJ86253A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2498-2026·2026-06-24
Medline Dr Fernandez procedure kits contain catheters failing performance specifications
Medline procedure kits labeled Dr Fernandez are being recalled because representative samples did not meet applicable catheter performance specifications. 91 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: DR FERNANDEZ, Medline kit number/SKU DYNJ68808
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2493-2026·2026-06-24
Medline procedure kits contain catheters failing performance specifications
Medline medical procedure kits including ECMO chest exploration, coronary artery bypass and D&C/cysto trays are being recalled because sample catheters did not meet performance specifications.
Product
MEDLINE Medical Procedure Kits labeled as: 1) CHEST EXPLORATION ECMO, Medline Kit Number/SKU DYNJ63789A; 2) CORONARY/ARTERY BYPASS TRAY, Medline Kit Number/SKU DYNJ17321G; 3) D&C/CYSTO, Medline Kit Number/SKU DYNJ909989B; 4) DDD LAPAROSCOPY PACK, Medline Kit Number/SKU D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2474-2026·2026-06-24
ConMed AirSeal 12mm palm grip 100mm ports may trigger overpressure alerts
ConMed AirSeal 12 mm Access Ports with Palm Grip Bladeless Optical Tip Obturators, 100 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide