State

California product recalls

72,966 recalls have nationwide distribution and so reach California. 13,246 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,246
Critical: 1,605
Severe: 2,843
Most recent: 2026-09-16

Of the 13,246 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,843 (21%) are Severe.

Which agencies issued them

These figures cover only the 13,246 recalls whose distribution notice names California specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5551–5575 of 86212

CriticalFDA (Devices)·Z-2617-2025·2025-10-08
Atlan A350XL anesthesia workstations recalled after piston ventilator failures during use
Draeger is recalling 223 Atlan A350XL anesthesia workstations that either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
Product
Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical ve
Category
Medical Device
Distribution
25 states
CriticalFDA (Devices)·Z-2667-2025·2025-10-08
MAGNETOM Vida MRI systems recalled over ice blockage in magnet venting
Siemens is recalling 498 MAGNETOM Vida (DE) MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2613-2025·2025-10-08
Reprocessed cardiac imaging catheters recalled over residual particulates on device surfaces
Medline is recalling 7,913 reprocessed ViewFlex Xtra ICE catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Product
Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2670-2025·2025-10-08
Surgical valve pack kits recalled after cannulas may not retain shape
Medline is recalling 828 VALVE PACK-LF kits because they contain lots of cannula products where the catheter may not retain its shape.
Product
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2665-2025·2025-10-08
MAGNETOM Verio Dot systems recalled over magnet venting ice blockage risk
Siemens is recalling 59 MAGNETOM Verio Dot systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Verio Dot. Model Number: 10684333.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2668-2025·2025-10-08
MAGNETOM Vida Fit MRI systems recalled over magnet vent ice blockage
Siemens is recalling 41 MAGNETOM Vida Fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Vida Fit. Model Number: 11410481.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2661-2025·2025-10-08
MAGNETOM Skyra fit MRI systems recalled over magnet vent ice blockage
Siemens is recalling 56 MAGNETOM Skyra fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Skyra fit. Model Number: 10849580.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2655-2025·2025-10-08
BIOGRAPH One scanner recalled over ice blockage in magnet venting system
Siemens is recalling one BIOGRAPH One (DE) system because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
BIOGRAPH One (DE). Model Number: 11689172.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2656-2025·2025-10-08
MAGNETOM Cima.X systems recalled over ice blockage in helium venting system
Siemens is recalling 22 MAGNETOM Cima.X (DE) systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
MAGNETOM Cima.X (DE). Model Number: 11647158.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2664-2025·2025-10-08
MAGNETOM Verio MRI systems recalled over magnet venting ice blockage risk
Siemens is recalling 154 MAGNETOM Verio MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Verio. Model Number: 10276755.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2611-2025·2025-10-08
Reprocessed cardiac mapping catheters recalled over residual particulates on device surfaces
Medline is recalling 7,913 reprocessed Webster CS 10-electrode catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Product
Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2658-2025·2025-10-08
MAGNETOM Lumina MRI systems recalled over helium venting ice blockage risk
Siemens is recalling 130 MAGNETOM Lumina (DE) MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
MAGNETOM Lumina (DE). Model Number: 11344916.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V672000·2025-10-08
BMW motorcycles recalled over cardan shaft that may lose drive power
BMW is recalling three 2026 R 1300 RT motorcycles whose cardan shaft may not have been sufficiently hardened, allowing the universal joint to slip and causing a loss of drive power.
Product
BMW — BMW R 1300 RT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V671000·2025-10-08
2026 BMW X6 and X4 Vehicles Recalled for Windshield Seal Defect
BMW is recalling 2026 X6 and X4 vehicles because the windshield may not be sealed properly, allowing water to enter electrical components and potentially causing loss of lights, door functions, or fire.
Product
BMW — BMW X6, X4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0030-2026·2025-10-08
Radiology software recalled because reports may not display fully when viewed
Change Healthcare is recalling 12 programs running Radiology Solutions software version 14.2.2 because a software issue means radiology reports may not be fully displayed.
Product
Change Healthcare Radiology Solutions software version 14.2.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0024-2026·2025-10-08
Reprocessed 1.7mm laser atherectomy catheters recalled over sterile barrier breaches
Northeast Scientific is recalling 616 reprocessed 1.7mm RX Turbo Elite laser atherectomy catheters because of potential breaches in the sterile barrier packaging.
Product
NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cle
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2639-2025·2025-10-08
Radiosurgery systems recalled over software defect that could cause collimator collision
Zap Surgical Systems is recalling 17 ZAP-X Radiosurgery Systems because a software defect could let the collimator collide with a patient's shoulders or the patient table.
Product
ZAP-X Radiosurgery System, Model: 300150
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0638-2025·2025-10-08
Shrimp cocktail bowls recalled over possible cesium 137 contamination at Kroger stores
Kroger is recalling 8,400 cases of shrimp cocktail bowls made under insanitary conditions in which the product may have been contaminated with Cesium-137.
Product
Shrimp Cocktail Bowl; 7oz clear plastic retail packaging. UPC: 011110622952 Shrimp Cocktail Bowl; 17oz clear plastic retail packaging. UPC: 011110624840
Category
Food
Distribution
16 states
HighFDA (Devices)·Z-0025-2026·2025-10-08
Reprocessed 2.0mm laser atherectomy catheters recalled for sterile packaging breaches
Northeast Scientific is recalling 141 reprocessed 2.0mm RX Turbo Elite laser atherectomy catheters because of potential breaches in the sterile barrier packaging.
Product
NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-159. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cle
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2637-2025·2025-10-08
Junctional tourniquet devices recalled over manufacturing defect affecting structural integrity
North American Rescue is recalling 552 Junctional Emergency Treatment Tools over a potential manufacturing defect that may compromise structural integrity and performance during use.
Product
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete (Modules 1-3), REF: 85-0550; KIT, TCCC MODULE ONE - SKILLS, REF: 85-0519; KIT, MULTI MISSION EXPEDITIONARY RESPONSE - MMERK, REF: 85-2420; KIT, TCCC SKILLS/IFAK
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25T017000·2025-10-08
Continental Recalls Specific Tires Due to Tread Detachment Risk
Continental is recalling specific tire models because the wrong rubber compound was used, which may cause the tread to detach and increase crash risk.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2673-2025·2025-10-08
Ophthalmic imaging software recalled over measured areas smaller than actual values
MedicalCommunications GmbH is recalling 474 units of HEYEX 2 / HEYEX PACS software because a measured value may be smaller than the actual area.
Product
Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0 (Build 2088) to 2.6.8 (Build 2220). Device Type: Software (Medical Image Management, Picture Archiving and Communication System)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0639-2025·2025-10-08
Frozen cooked shrimp bags recalled over possible cesium 137 contamination
Kroger is recalling 4,871 cases of frozen cooked tail-on shrimp made under insanitary conditions in which the product may have been contaminated with Cesium-137.
Product
16/25 Frozen Cooked Tail-On Farm Raised Shrimp; 12oz clear plastic retail bag. UPC: 011110649812 51/60 Frozen Cooked Tail-On Farm Raised Shrimp; 32oz clear plastic retail bag. UPC: 011110967015
Category
Food
Distribution
16 states
HighFDA (Devices)·Z-0023-2026·2025-10-08
Reprocessed 1.4mm rapid exchange atherectomy catheters recalled for packaging breaches
Northeast Scientific is recalling 1,019 reprocessed 1.4mm RX Turbo Elite laser atherectomy catheters because of potential breaches in the sterile barrier packaging.
Product
NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cle
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0036-2026·2025-10-08
Vascular grafts recalled after delamination reports prompt instructions for use update
W. L. Gore is recalling 52,306 GORE ACUSEAL Vascular Grafts following reports of graft delamination, and is updating the instructions for use with expanded warnings.
Product
GORE ACUSEAL Vascular Graft, REF: ECH050020J, ECH050020W, ECH050050J, ECH050050W, ECH060010A, ECH060020A, ECH060020J, ECH060020W, ECH060040, ECH060040A, ECH060040W, ECH060050A, ECH060050J, ECH460045A, ECH460045J, ECH470045, ECH470045A; used with Instructions for Use.
Category
Medical Device
Distribution
51 states