State

California product recalls

73,566 recalls have nationwide distribution and so reach California. 13,263 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,263
Critical: 1,605
Severe: 3,368
Most recent: 2026-10-21

Of the 13,263 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 3,368 (25%) are Severe.

Which agencies issued them

These figures cover only the 13,263 recalls whose distribution notice names California specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24676–24700 of 86829

SevereFDA (Devices)·Z-0694-2022·2022-03-16
Medtronic TurboHawk Plus Directional Atherectomy System Recalled Due to Design Defect
ev3 Inc. is recalling the Medtronic TurboHawk Plus Directional Atherectomy System due to design similarities to a device with reported tip detachment and embolization incidents. The FDA has classified this as a Class I recall.
Product
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Multi-vessel, Catalog number THP-M. For use in peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0695-2022·2022-03-16
Medtronic TurboHawk Plus atherectomy system recalled for potential tip detachment
The Medtronic TurboHawk Plus Directional Atherectomy System (catalog THP-S) is being recalled due to design similarities to another device that experienced tip detachment and embolization. The recall affects 245 devices distributed nationwide.
Product
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For use in peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0851-2022·2022-03-16
Del Monte Bubble Fruit cups recalled for potential metal fragments
DEL MONTE FOODS INC is recalling Del Monte Bubble Fruit Tropical Mixed Fruit Cup Snacks due to potential metal fragments approximately 2–3 mm in size. No injuries have been reported.
Product
Del Monte Bubble Fruit - Tropical Mixed Fruit Cup Snacks. Mixed fruit and popping boba with sweetened juice. 3.5 0z (4 pack), 6 x 4 pack sleeves per carton UPC: 24000 25236
Category
Food
Distribution
29 states
HighFDA (Food)·F-0829-2022·2022-03-16
Factor 75 Chili Meal Recalled for Undeclared Milk Allergen
Factor 75 Fiery Beef & Black Bean Chili meals are being recalled due to undeclared milk allergen. The product was distributed nationwide and may affect consumers with milk allergies.
Product
Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer
Category
Food
Distribution
49 states
HighFDA (Devices)·Z-0733-2022·2022-03-16
ExacTrac Dynamic Software Yaw Angle Error May Affect Radiotherapy Positioning
ExacTrac Dynamic radiotherapy positioning software (versions 1.0.0–1.0.3) may calculate incorrect yaw angle for patient positioning with Varian linear accelerators, potentially affecting cone-beam CT imaging setup accuracy during radiotherapy.
Product
ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning and Moni. 1.0.1 INST; 20910-01B, ETD Positioning and Moni. 1.0.2 INST; and 20910-01C ETD Positioning and Moni. 1.0.3 INST.
Category
Medical Device
Distribution
20 states
HighFDA (Food)·F-0825-2022·2022-03-16
LUPAG Dried Salted Plums Recalled for Elevated Lead Levels
LUPAG brand Plain Dried Salted Plums are being recalled by Rojas Inc. due to elevated lead levels. Consumers should not eat this product.
Product
LUPAG brand Plain Dried Salted Plums, net wt. 0.5oz, pre-priced at $.99 packaged in transparent poly bags sealed with a cardboard header, stapled one dozen packages on a cardboard strip. UPC 7 25535 01133 7. Ingredients: Dried Prunes, salt. Origin: Taiwan or China Rojas…
Category
Food
Distribution
1 state
HighNHTSA·22V163000·2022-03-16
2022 Volkswagen Golf R engine design cover fire risk recall
The engine design cover in 2022 Volkswagen Golf R vehicles may loosen during high acceleration and contact hot engine surfaces, increasing fire risk. Dealers will remove it free of charge.
Product
VOLKSWAGEN — VOLKSWAGEN GOLF R, GTI
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0741-2022·2022-03-16
FISH Diagnostic Probe Kit Color Labeling Error Affects Test Results
Cytocell Ltd. is recalling a Del(5q) Deletion FISH Probe Kit due to incorrect color labeling on probe components. The mislabeling may cause misinterpretation of test results for patients with AML or MDS.
Product
Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0727-2022·2022-03-16
B. Braun dispensing pins recalled for air filter leakage risk
B. Braun Medical is recalling dispensing pins with an elevated leakage risk in the air inlet filter. The leakage may reduce medication doses, delay treatment, or contaminate the fluid path, potentially causing bloodstream infection.
Product
Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration or injection of medication or enteral feeding solution from inverted multi-dose vials.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0743-2022·2022-03-16
Medtronic endotracheal tubes recalled due to manufacturing nonconformity
Medtronic Xomed is recalling over 301,000 NIM TRIVANTAGE EMG Endotracheal Tubes due to a manufacturing nonconformity. These devices were distributed worldwide.
Product
NIM TRIVANTAGE EMG Endotracheal Tube
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0725-2022·2022-03-16
Philips X-ray System Cooling Leak Poses Fire Risk
Philips Allura CV20 X-ray systems with certain Laird chillers may leak cooling liquid onto electrical components, potentially causing fire or smoke. Affected systems should not be operated until the issue is addressed.
Product
Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0732-2022·2022-03-16
Radiation therapy planning software displays wrong images during animation playback
RayStation/RayPlan versions 6.0.0.24 through 9.2.0.483 incorrectly display selected images as both primary and secondary when animation playback is running, affecting treatment planning visualization.
Product
RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 .…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0724-2022·2022-03-16
Philips Allura Xper X-ray systems cooling system leak poses fire risk
Philips Allura Xper interventional X-ray systems may experience cooling liquid leaks that could drip on electrical components, creating risk of fire, smoke, or burning odors. No injuries have been reported.
Product
Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray: Model Number: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2022·2022-03-16
FDA Recalls Diagnostic Test Strips for False Positive Results
NeuMoDx COVID-19 test strips (Lot 116305 S/L-02) are recalled due to product contamination that increases risk of false positive results. The recall affects 102 boxes distributed in FL, MD, MI, and NY.
Product
NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947). Distributed in boxes of 6 assay strips in individual pouches. Box, pouch and strips all labeled with product name, ref #, lot #, and expiration date.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0739-2022·2022-03-16
Nextra CH Hammertoe Surgical Implant Kit Recalled for Locking Mechanism Defect
Nextremity Solutions recalls the Nextra CH Hammertoe Mini Instrument Kit for a defect that may deform the implant's locking mechanism during insertion, potentially requiring revision surgery.
Product
Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0830-2022·2022-03-16
American Gourmet Saladitos Recalled for High Lead Levels
American Gourmet Saladitos dried salted plums are recalled due to high lead levels detected by California health officials. The 1.5 oz. packages distributed in California should not be consumed.
Product
American Gourmet Saladitos (Dried Salted Plums) 1.5 oz. package UPC: 1578600104
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0729-2022·2022-03-16
Vascular Graft Mislabeled; Packaging Labels Do Not Match Product Specifications
A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.
Product
HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0856-2022·2022-03-16
Dry Salted Plum with Chili Products Recalled for Potential Lead Contamination
El Super Leon and El Leoncito brand Dry Salted Plum with Chili products are recalled due to potential lead contamination. Consumers should not consume these products.
Product
El Super Leon brand, Dry Salted Plum with Chili, Shelf Stable, packaged in plastic bag, Net Wt 1.05oz, UPC 8-52605-00408. With 12 packs of 12 units per case, for a total of 144 units per case. El Leoncito brand, Dry Salted Plum with Chili, Shelf Stable, packaged in plastic bag…
Category
Food
Distribution
6 states
HighCPSC·22103·2022-03-16
B. toys Wooden Activity Walker recalled for choking hazard
B. toys Walk 'n' Learn wooden toddler walkers are being recalled because wheels and attachment hardware can detach in small pieces, creating a choking hazard for young children. Battat has received six reports of detachment, including one incident where a child placed a detached metal nut in her mouth.
Product
B. toys Wooden Activity Walker - Walk 'n' Learn
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V162000·2022-03-16
2021 Volkswagen ID.4 Battery Cell Soldering Defect Recall
Volkswagen is recalling certain 2021 ID.4 vehicles due to improper soldering of the high-voltage battery connection. The defect may cause an unreliable connection that could lead to vehicle stalling and increase crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0823-2022·2022-03-16
El Chavito Saladitos Enchilados Salted Plums Recalled for Potential Lead Contamination
El Chavito Saladitos Enchilados Salted Plums (1.7 oz.) are being recalled nationwide due to potential lead contamination. Consumers should not consume this product.
Product
El Chavito¿ Saladitos Enchilados Salted Plums with Chili, net wt. 1.7 oz., Individual UPC 859470006070, Master Case UPC 859470006612.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0740-2022·2022-03-16
Surgical hammertoe instruments recalled for potential locking mechanism deformation
The Nextra Cannulated Hammertoe Standard Instrument Kit's driver may deform the implant locking mechanism during insertion, potentially requiring revision surgery.
Product
Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0828-2022·2022-03-16
Dried Salted Plums Recalled for Elevated Lead Levels
Pacific Golden Coast Trading Inc is recalling 820 cases of dried salted plums due to elevated lead levels. The product was distributed in California and Texas.
Product
Dried salted plum, packaged in 22 lbs. carton. Product of China.
Category
Food
Distribution
2 states
HighFDA (Food)·F-0855-2022·2022-03-16
Dry Salted Plums Recalled Due to Potential Lead Contamination
El Super Leon Ponchin Snacks is recalling EL Leoncito and El Super Leon brand dry salted plums due to potential lead contamination. Consumers should not consume these products.
Product
EL Leoncito brand Dry Salted Plum, Shelf Stable, packaged in plastic bag, Net Wt 1.4oz, UPC 8-52605-00024. 12 packs with 12 units per case - 144 total units El Super Leon brand Dry Salted Plum, Shelf Stable, packaged in plastic bag, Net Wt 1.4oz, UPC 8-52605-00407. The label…
Category
Food
Distribution
6 states
HighFDA (Food)·F-0821-2022·2022-03-16
La Fiesta Salted Plums with Chili Recalled for Elevated Lead Levels
La Fiesta brand Salted Plums with Chili are being recalled due to elevated lead levels in the product. The recall affects 8,304 packages distributed across Arkansas, California, Georgia, North Carolina, Nevada, Oklahoma, and Utah.
Product
La Fiesta brand, Salted Plums with Chili Product. Product is packaged in cello bags, net wt. 1oz. UPC 0 32327 02829 0. There are 8 dozens per case. Product is labeled in parts: "***SALADITOS CON CHILE *** SALTED PLUMS WITH CHILI ***PRODUCT OF CHINA***Distributed By: La Fiesta…
Category
Food
Distribution
7 states