Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent Product Recall Alerts List
Showing 851 - 875 of 4,622 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08 PEDINTS10 UDI code: 00801741183300¿ 10801741183307 00801741183218¿ 10801741183215 00801741183232 10801741183239 00801741183225¿ 10801741183222 00801741183249 10801741183246 00801741183263¿ 10801741183260 00801741183270¿ 10801741183277 00801741183287¿ 10801741183284 Preamendment REF: INTL14 INTL15 INTL16 INTP14 UDI code: 00801741183164¿ 10801741183161 00801741183171¿ 10801741183178 00801741183188 10801741183185 00801741183294 10801741183291 For urological u
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
|
FDA
Z-3117-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jun 25, 2026
|
Details |
|
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
|
FDA
Z-3106-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jul 23, 2026
|
Details |
|
Halyard IV Start Kit Non-Sterile REF: KRIV26-02
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.
|
FDA
Z-3109-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jul 14, 2026
|
Details |
|
Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
|
FDA
Z-3107-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jul 23, 2026
|
Details |
|
AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B
The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation.
|
FDA
Z-3138-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jul 29, 2026
|
Details |
|
MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))
Hemodialysis concentrates contain high endotoxin levels
|
FDA
Z-3134-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Aug 5, 2026
|
Details |
|
Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 00801741143243 SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300316AC UDI-DI code: 00801741143250 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care¿ REF: A319516AMC UDI-DI code: 00801741143472 SureStep" Foley Tray System Bard¿ Lubricath Foley REF: A800366C UDI-DI code: 00801741143571 SureStep" Foley Tray System Bard¿ Silicone Foley Catheter Tray REF: A897514C UDI-DI code: 00801741074011¿ SureStep" Foley Tray System Bard¿ Silicone Foley Ca
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
|
FDA
Z-3119-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jun 25, 2026
|
Details |
|
Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)
Hemodialysis concentrates contain high endotoxin levels
|
FDA
Z-3136-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Aug 5, 2026
|
Details |
|
Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028), 2. 36FR(15036);
An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.
|
FDA
Z-3113-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Aug 7, 2026
|
Details |
|
Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801¿ 10801741024808 00801741024818¿ 10801741024815 00801741024825¿ 10801741024822 SureStep" Foley Tray System with Bardex¿ Lubricath Temp Sensing Foley Catheter REF: A119416M UDI code: 00801741073700 10801741073707 SureStep" Foley Tray System Bard¿ Lubricath Foley REF: A800361 UDI code: 00801741073939 10801741073936 SureStep" Foley Tray System Bard¿ Lubricath¿ Foley Catheter Tray REF: A899616 UDI code: 00801741104534¿ 10801741104531 SureStep" Foley Tray System Bardex¿
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
|
FDA
Z-3114-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jun 25, 2026
|
Details |
|
HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, US English with Gateway - 2 Min CPR UDI-DI code: 0506016712804 HeartSine SAM 360P 360P US Device, US English - 2 Min CPR UDI-DI code: 0506016712068 HeartSine SAM 450P SAM 450P US Device, US English (2 min CPR) UDI-DI code: 0506016712069 The HeartSine samaritan¿ PAD (Public Access Defibrillator) Models SAM 350P, SAM 360P and SAM 450P are indicated for use on victims of cardiac arrest who are exhibiting the fol
Due to a damaged (over stretched) membrane tail that causes an intermittent fault.
|
FDA
Z-3120-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jul 27, 2026
|
Details |
|
Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 947316 947318 UDI codes: 00801741024924¿ 10801741024921 00801741024931¿ 10801741024938 00801741024948¿ 10801741024945 Lubri-Sil¿ I.C. Complete Care¿ All-Silicone Foley Catheter Tray REF: 300416A UDI code: 00801741024580 10801741024587 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care¿ REF: A300416A UDI code: 00801741073762¿ 10801741073769 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care REF: A303416A UDI code: 00801741073823 10801741073820 SureStep" Foley Tray System
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
|
FDA
Z-3115-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jun 25, 2026
|
Details |
|
Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR(8028), 4. 32FR(8032), 5. 36FR(8036);
An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.
|
FDA
Z-3111-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Aug 7, 2026
|
Details |
|
Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 10801741121064 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A304400A UDI code: 00801741073847¿ 10801741073844 SureStep" Foley Tray System Add-A-Foley Catheter REF: A399400 UDI code: 00801741100369¿ 10801741100366 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A399400A UDI code: 00801741073915¿ 10801741073912 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A904400A UDI code: 00801741074097¿ 1080174107
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
|
FDA
Z-3118-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Jun 25, 2026
|
Details |
|
Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at wavelengths of 532 nm and 1064 nm through a fiber-optic handpiece. The system may be configured with an Intelligent Cooling Device (ICD) to provide epidermal cooling during laser treatment
Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.
|
FDA
Z-3110-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Aug 6, 2026
|
Details |
|
MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201
Hemodialysis concentrates contain high endotoxin levels
|
FDA
Z-3133-2026
|
Medical Device | High |
Sep 16, 2026
Recall: Aug 5, 2026
|
Details |
|
Incorrect Tires Installed
Grand Design RV, LLC (Grand Design) is recalling certain 2026-2027 Lineage recreational vehicles equipped with the optional Lineage 43 tire package. The vehicle's top speed may exceed the tire's speed rating. A tire may fail while traveling at higher speeds, increasing the risk of a crash.
|
NHTSA
26V595000
|
Vehicle | High |
Sep 14, 2026
Recall: Sep 14, 2026
|
Details |
|
Loss of Steering Control from Bolt Failure
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2018 Tiguan, 2018-2019 Atlas, and 2019-2021 Audi Q3 vehicles. One of the bolts that attaches the steering rack to the subframe may corrode and break. If this happens, the steering rack housing can break. A broken steering rack housing can result in a loss of steering control, increasing the risk of a crash.
|
NHTSA
26V590000
|
Vehicle | High |
Sep 11, 2026
Recall: Sep 11, 2026
|
Details |
|
Wiring Harness May Become Damaged and Cause a Loss of Drive Power
Micro Bird USA LLC (Micro Bird) is recalling certain 2025-2027 G5e school buses. A wiring harness may have been incorrectly routed. A metal bracket may contact and damage the harness, causing a loss of drive power. A loss of driver power increases the risk of a crash.
|
NHTSA
26V591000
|
Vehicle | High |
Sep 11, 2026
Recall: Sep 11, 2026
|
Details |
|
Wiring Harness May Become Damaged and Cause a Loss of Drive Power
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2025-2026 G5e transit buses. A wiring harness may have been incorrectly routed. A metal bracket may contact and damage the harness, causing a loss of drive power. A loss of driver power increases the risk of a crash.
|
NHTSA
26V593000
|
Vehicle | High |
Sep 11, 2026
Recall: Sep 11, 2026
|
Details |
|
Wiring Harness May Become Damaged and Cause a Loss of Drive Power
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2025-2026 G5e school buses. A wiring harness may have been incorrectly routed. A metal bracket may contact and damage the harness, causing a loss of drive power. A loss of driver power increases the risk of a crash.
|
NHTSA
26V594000
|
Vehicle | High |
Sep 11, 2026
Recall: Sep 11, 2026
|
Details |
|
Roof Rack Crossbars May Detach
Chrysler (FCA US, LLC) is recalling certain 2022-2025 Jeep Wagoneer, 2022-2026 Jeep Grand Wagoneer, 2023-2025 Jeep Wagoneer L, and 2023-2026 Jeep Grand Wagoneer L vehicles. The pivot bolts for the roof rack crossbars may not have been tightened properly, allowing them to detach. Detached roof rack crossbars can create a road hazard, increasing the risk of a crash.
|
NHTSA
26V584000
|
Vehicle | High |
Sep 10, 2026
Recall: Sep 10, 2026
|
Details |
|
Roof Rack Crossbars May Detach
Chrysler (FCA US, LLC) is recalling certain MOPAR roof rack kits with part numbers 68747056AA, 68529228AA, 68529228AB, 68442426AA, 68442426AB, and 68442426AC. The pivot bolts for the roof rack crossbars may not have been tightened properly, allowing them to detach. Detached roof rack crossbars can create a road hazard, increasing the risk of a crash.
|
NHTSA
26E064000
|
Vehicle | High |
Sep 10, 2026
Recall: Sep 10, 2026
|
Details |
|
Incorrectly Labeled Tire Sidewall/FMVSS 110
Wheel Pros, LLC (Wheel Pros) is recalling certain Avix TrailTek RT, size 35X12.50R20LT tires. The tire sidewall may be incorrectly labeled "Not for Highway Use." As such, these tires fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, "Tire Selection and Rims." Incorrectly labeled tires may increase the risk of a crash.
|
NHTSA
26T014000
|
Vehicle | High |
Sep 10, 2026
Recall: Sep 10, 2026
|
Details |
|
Rearview Camera Image May Not Display
Forest River Bus, LLC (Forest River) is recalling certain 2019-2022 Lone Star Vans built on Ram ProMaster chassis. Cracks in the microprocessor may cause the rearview camera image not to display properly. A rearview image that does not display properly reduces the driver's view behind the vehicle, increasing the risk of a crash.
|
NHTSA
26V585000
|
Vehicle | High |
Sep 10, 2026
Recall: Sep 10, 2026
|
Details |
Recent Product Recall Alerts
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