State

California product recalls

72,940 recalls have nationwide distribution and so reach California. 13,245 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,245
Critical: 1,605
Severe: 2,843
Most recent: 2026-09-09

Of the 13,245 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 13,245 recalls whose distribution notice names California specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5076–5100 of 86185

CriticalFDA (Food)·H-0150-2026·2025-10-29
Breakfast burritos and wraps recalled after egg ingredient tested positive for Listeria
M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.
Product
Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0095-2026·2025-10-29
Kroger penne salad recalled over Listeria in recalled pasta ingredient
Kroger is recalling 25,792 lbs of store-made Smoked Mozzarella Penne Salad because it contains a pasta ingredient recalled for potential Listeria monocytogenes.
Product
Smoked Mozzarella Penne Salad, packaged in plastic containers with various weights, with UPC 227573-1XXXX (sold at deli service counters) or UPC 227573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fry
Category
Food
Distribution
28 states
CriticalFDA (Food)·H-0126-2026·2025-10-29
Store-made penne pasta salad recalled over Listeria in pasta ingredient
Albertsons Companies is recalling Ready Meals Smoked Mozzarella Penne Pasta Salad because the store-made deli item contains a penne pasta ingredient recalled for Listeria monocytogenes.
Product
Ready Meals Smoked Mozzarella Penne Pasta Salad, UPC 291298 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK.
Category
Food
Distribution
15 states
CriticalFDA (Food)·H-0119-2026·2025-10-29
Store-made pesto bowtie salad recalled over Listeria in pasta ingredient
Albertsons Companies is recalling Basil Pesto Bowtie Pasta Salad sold under its California, Hawaii and Nevada banners because it contains a bowtie pasta ingredient recalled for Listeria.
Product
Basil Pesto Bowtie Pasta Salad, UPC 216492 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Andronico's Community, Markets, Pak'N Save, Safeway, and Vons in CA, HI, and NV.
Category
Food
Distribution
15 states
CriticalFDA (Devices)·Z-0154-2026·2025-10-29
IV burette sets recalled over missing internal shutoff valve component
ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.
Product
IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B9213; 70" (178 cm) 150 ml Burette Set (Clave, Shut-Off) w/3-Way Stopcock, Clave, Graduated Adapter,
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0070-2026·2025-10-29
Hemodialysis bloodline sets recalled over micro air bubbles from damaged connectors
B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.
Product
Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG Model/Catalog Number: SL-2010M2096 Software Version: N/A Product Description: STREAMLINE BLOODLINE SET FOR DIALOG Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0125-2026·2025-10-29
Penne salad kits recalled over Listeria in recalled pasta ingredient
Albertsons Companies is recalling its store-made Smoked Mozzarella Penne Salad Kit because it contains a penne pasta ingredient recalled for Listeria monocytogenes.
Product
Smoked Mozzarella Penne Salad Kit, UPC 271876 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK.
Category
Food
Distribution
15 states
CriticalFDA (Food)·H-0149-2026·2025-10-29
Breakfast burritos recalled after cooked egg ingredient tested positive for Listeria
M.C.I. Foods is recalling 330 cases of Cheese and Egg with Green Salsa Breakfast Burritos after the cooked egg ingredient tested positive for Listeria monocytogenes.
Product
Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0117-2026·2025-10-29
Pesto bowtie pasta salad recalled over Listeria in recalled ingredient
Albertsons Companies is recalling Ready Meals Pesto Bowtie Pasta Salad sold under six banners because it contains a bowtie pasta ingredient recalled for Listeria monocytogenes.
Product
READY MEALS Pesto Bowtie Pasta Salad, UPC 27133 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Pavilions, Randalls, Safeway, Tom Thumb, and Vons in AR, AZ, CA, CO, LA, NE, NM, NV, OK, SD, TX, UT
Category
Food
Distribution
15 states
SevereNHTSA·25V737000·2025-10-29
Mazda CX-50 front suspension bolts may allow wheel detachment
Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.
Product
MAZDA — MAZDA CX-50, CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0240-2026·2025-10-29
Veritor Connect software recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the BD Veritor Plus Analyzer to BD Synapsys.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V738000·2025-10-29
Prevost Recalls 2025 X3-45 Commuter Buses Due to Seat Belt Anchorage Defect
Prevost is recalling 2025 X3-45 Commuter buses because improperly installed wheelchair seat belt anchorages may detach in a crash, increasing injury risk.
Product
PREVOST — PREVOST X3-45 COMMUTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0216-2026·2025-10-29
Immunoassay analyzers recalled over dilution factor anomaly affecting patient results
Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxI 9000 Access Immunoassay Analyzer, Part Number C11137
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0206-2026·2025-10-29
ENFit sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2026·2025-10-29
Gastric sump anti-reflux valves recalled after breakage complaints from excessive force
Cardinal Health is recalling all lots of Salem Sump Anti-Reflux Valves after complaints of valve breakage due to excessive force during use, and is providing additional guidance for use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0231-2026·2025-10-29
ECG trunk cables recalled because improper module placement can cause overheating
GE is recalling 29,225 MAC VU360 acquisition trunk cables and module holders because incorrect placement of the module can wear the cable until it overheats in use.
Product
MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0215-2026·2025-10-29
Clinical analyzer modules recalled over dilution factor software anomaly affecting results
Beckman Coulter is recalling 160 DxC 500i Clinical Analyzer modules over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0208-2026·2025-10-29
Silicone stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0113-2026·2025-10-29
Frozen raw shrimp recalled across four brands over cesium 137 contamination
Southwind Foods is recalling frozen raw shrimp sold under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.
Product
Arctic Shores; Best Yet; Great American; Master Catch branded Frozen Raw shrimp; 2lbs; 1lbs; UPC: 041130810923; 041512179471; 041130810978; 041130811029; 011110641182; 829944010636; 041130811333; 041130810916; 041130812460; 041130810824; 829944012463; 829944012012; 829944004079
Category
Food
Distribution
34 states
HighFDA (Drugs)·D-0097-2026·2025-10-29
Opdualag injection vials recalled from one lot over sterility assurance
Bristol-Myers Squibb is recalling 12,778 vials of Opdualag (nivolumab and relatlimab-rmbw) injection from one lot for lack of assurance of sterility.
Product
OPDUALAG — OPDUALAG (NIVOLUMAB AND RELATLIMAB-RMBW)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0227-2026·2025-10-29
Bipolar hip heads recalled downstream after femoral components failed transit testing
Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.
Product
iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0235-2026·2025-10-29
Microbiology data systems recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2. COMPUTER OPTIPLEX EPICENTER SPARE, Catalog Number: 441421. 3. Generic NUC 2, Catalog Number: 445398. 4. Nuc 5i5 Os Image Bow 2.X, C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0232-2026·2025-10-29
Insulin pumps recalled over software defect causing unexpected correction bolus
Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.
Product
t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0233-2026·2025-10-29
Oral thermometer probes recalled after being programmed with rectal configuration
Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.
Product
Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0035-2026·2025-10-29
Alcohol prep pads recalled from one lot as a subpotent drug
Medline is recalling 222,800 alcohol prep pads from one lot because the product is subpotent.
Product
Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30.
Category
Drug
Distribution
Distributed nationwide