State

California product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7626–7650 of 86230

HighFDA (Devices)·Z-1654-2025·2025-04-30
Abbott CELL-DYN Ruby hematology analyzer affected by expired reagent date masking
Abbott is recalling the CELL-DYN Ruby hematology analyzer because expired reagents may have their expiration dates automatically changed to current or future dates without user notification, potentially leading to use of expired reagents.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-10 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1639-2025·2025-04-30
BD PYXIS MEDBANK Automated Dispensing Cabinet Software Defect
CareFusion's BD PYXIS MEDBANK and MEDFLEX automated dispensing cabinets may experience a software issue during bin restocking that doubles bin quantities, potentially delaying access to medications and supplies.
Product
BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI 1HH-1HM-1FM, 169-102; MINI 2FH, 138902-01; MINI 2FH, 169-104; MINI 2FM, 169-105; MINI 2HH-1FH, 169-106; MINI 2HH-1FH, 138908-01; MINI 2HH-1FM, 169-107; MINI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1655-2025·2025-04-30
CELL-DYN Ruby hematology analyzer system expiration date validation
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers (model 08H67-13) because expired reagents can be used without proper notification when their expiration dates are scanned or entered into the system.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-13 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0734-2025·2025-04-30
S Martinelli Apple Juice Recalled for Potential Patulin Contamination
S Martinelli & Company is recalling approximately 7,234 cases of apple juice in 10 oz bottles due to potential contamination with patulin. Consumers who have purchased affected product should not consume it.
Product
Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack; 6 packs per case)
Category
Food
Distribution
28 states
HighFDA (Devices)·Z-1622-2025·2025-04-30
VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System C-Ring Break
Maquet Cardiovascular is recalling the VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System due to a ceramic C-Ring component that may break during use. At least 12 user complaints were reported as of March 3, 2025.
Product
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm extended length endoscope. The Harvesting Cannula has four lumens which house the endoscope, C-Ring, distal lens washer tube, and Harvesting Tool for cutting and cauterizin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1663-2025·2025-04-30
Skytron Freedom Monitor Mount Hardware Recall for Inadequate Thread Engagement
The mounting hardware supplied with the Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount does not provide adequate thread engagement to support the weight of the frame and monitor, creating a risk of hardware failure and separation.
Product
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1653-2025·2025-04-30
CELL-DYN Ruby hematology analyzer expiration date software defect
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because a software defect allows expired reagents to be used without user notification. The system may incorrectly update expiration dates to current or future dates, contrary to the operator's manual.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-03 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1583-2025·2025-04-30
Zenition 70 Medical Device Recall: Unintended Radiation Exposure Risk
Philips is recalling Zenition 70 systems with Vascular Extension option and Wireless Foot Switch due to potential for unintended radiation exposure in healthcare facilities.
Product
Zenition 70. The device is to be used in health care facilities both inside and outside the operating room, sterile as well as non-sterile environment in a variety of procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0370-2025·2025-04-30
Glycopyrrolate 1mg/5mL Syringes Recalled for Sterility Risk
Denver Solutions, LLC (DBA Leiters Health) is recalling Glycopyrrolate 1mg/5mL single-dose syringes (Lot #2431015B, expiration 4/10/2025) distributed nationwide because some syringes were found to be leaking or damaged, which compromises sterility assurance.
Product
Glycopyrrolate, 1mg per 5mL, (0.2 mg/mL), Single Dose 5 mL syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC 71449-104-11
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1660-2025·2025-04-30
Philips Brilliance CT Big Bore X-Ray System Gantry Motion Collision Hazard
Philips is recalling Brilliance CT Big Bore computed tomography systems due to unintended motion in the interventional control that may cause the gantry or table to collide with operators or patients.
Product
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1657-2025·2025-04-30
Globus Medical MAGEC 2 Rod recalled for incorrect outer diameter assembly
Globus Medical is recalling MAGEC 2 Rod model MC2-5090S devices because certain units were assembled with a 5.5mm outer diameter rod instead of the required 5.0mm specification.
Product
MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1645-2025·2025-04-30
Zimmer Biomet Ceramic Hip Prosthesis Head Lacks Stem Compatibility Information
Zimmer, Inc. is recalling a ceramic hip prosthesis head because its labeling does not adequately describe compatibility with cobalt-chrome or stainless-steel femoral stems.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +0 Neck, Model Number 802602202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0731-2025·2025-04-30
Gold Garlic Powder Irradiated Recalled for Potential Metal Contamination
Pacific Meridian Group, LLC is recalling Gold Garlic Powder Irradiated due to potential contamination with foreign objects (metal). The recalled product was distributed in CA, IL, and TX.
Product
GOLD GARLIC POWDER IRRADIATED; NET WT. 50 LBS; PRODUCT OF CHINA
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0740-2025·2025-04-30
Frozen Chopped Cilantro Recalled for Potential Foreign Object Contamination
Supherb Farms is recalling frozen chopped cilantro due to potential contamination with foreign objects. Consumers should not use the product and should discard it or return it to the retailer.
Product
Label: FROZEN CHOPPED CILANTRO; PACK SIZE: 4 - 8 oz; NET WT: 2 lb; PERISHABLE - KEEP FROZEN; Packaging: 4 - 8 oz ziploc plastic bags in a white cardboard box; Net Wt. 2 lb
Category
Food
Distribution
8 states
ModerateFDA (Food)·F-0739-2025·2025-04-30
IQF Cilantro Large Recalled Due to Foreign Object Contamination
Supherb Farms is recalling frozen cilantro (IQF Cilantro Large, 30 lb packages) distributed across the United States, Canada, and Mexico due to potential contamination with foreign objects.
Product
Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blue plastic liner inside brown cardboard box
Category
Food
Distribution
8 states
ModerateFDA (Devices)·Z-1641-2025·2025-04-30
Merit Medical EsophyX Z+ Fastener Delivery Device Instructions Update
Merit Medical has updated instructions for the EsophyX Z+ fastener delivery device to provide additional information about risks associated with device over-rotation and multiple fastener deployment.
Product
Merit Medical , REF: R2275, EsophyX Z+ with SerosaFuse Implantable Fasteners, (1) Fastener Delivery Device, (2) 7.5mm Cartridges, STERILEEO,RxOnly
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1649-2025·2025-04-30
Zimmer Biomet Ceramic Hip Head 22.2 mm Lacks Stem Compatibility Information
Zimmer, Inc. is recalling a ceramic hip prosthesis head because the product labeling does not adequately describe compatibility with certain femoral stems used in hip replacement surgery.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1666-2025·2025-04-30
Tempus Pro Patient Monitor software error when using video laryngoscope
Remote Diagnostic Technologies Ltd. is recalling Tempus Pro Patient Monitors due to a software issue that causes an error screen when a video laryngoscope is attached to the device.
Product
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset dock), 00-1024-R (Tempus Pro printer), 00-1026-R (Tempus Pro printer, IBP), 00-1007 [(Tempus Pro, BT Dock (IB Only)],
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1646-2025·2025-04-30
Zimmer Biomet Ceramic Femoral Head Hip Prosthesis Labeling Recall
Zimmer, Inc. is recalling a ceramic femoral head hip prosthesis (Model 802602203) because product labeling lacks compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +3 Neck, Model Number 802602203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1647-2025·2025-04-30
Zimmer Biomet Ceramic Hip Prosthesis Heads Lack Stem Compatibility Information
Zimmer, Inc. is recalling Zimmer Biomet Ceramic Head hip prostheses (Model 802802201, 22.2 mm diameter) because product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 802802201; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1640-2025·2025-04-30
Merit Medical EsophyX Z+ Fastener Delivery Device Safety Update
Merit Medical is updating instructions for the EsophyX Z+ Fastener Delivery Device due to risks associated with device over-rotation and multiple fastener deployment.
Product
Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0385-2025·2025-04-30
HYDROmorphone Hydrochloride 50 mg Cassettes Recalled for Superpotency
OurPharma LLC is recalling HYDROmorphone Hydrochloride 50 mg/50 mL cassettes nationwide because the assay results showed higher potency than specification.
Product
HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1040-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1659-2025·2025-04-30
Radiometer ABL90 Series Blood Analyzers May Unexpectedly Freeze
Radiometer ABL90 FLEX and ABL90 FLEX PLUS analyzers running Windows 10 versions RWIN10 1.0 and RWIN10 1.1 may freeze unexpectedly during sample measurement, causing test results to be lost and delayed.
Product
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090 Radiometer ABL90 Series - Radiometer ABL90 FLEX PLUS Model Number 393-092 The Radiometer ABL90 Series is a portable, automated analyzer for use in the laboratory environment, near patients or point-of-care
Category
Medical Device
Distribution
49 states
ModerateFDA (Drugs)·D-0388-2025·2025-04-30
Duloxetine Delayed-Release Capsules Recalled for Nitrosamine Impurity
Breckenridge Pharmaceutical is recalling Duloxetine Delayed-Release Capsules 30 mg nationwide due to the presence of a nitrosamine drug substance related impurity above proposed interim limits.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0386-2025·2025-04-30
Bimatoprost Bulk Powder Recalled by Medisca for CGMP Deviations
Medisca Inc. is voluntarily recalling Bimatoprost bulk powder in three sizes due to manufacturing process deviations. The powder was distributed nationwide.
Product
Bimatoprost powder, Bulk Ingredient, a) 5g (NDC 38779-3066-03), b) 1g (NDC 38779-3066-06), c) 1g (NDC 38779-3066-09) drums, Medisca, Plattsburgh, NY
Category
Drug
Distribution
Distributed nationwide