State

California product recalls

20,364 recalls have nationwide distribution and so reach California. 0 additional recalls listed California specifically in their distribution scope.

About recalls in California

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect California consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14626–14650 of 20364

HighFDA (Devices)·Z-0943-2023·2023-01-18
McCormick Medical Distribution PORT TRAY recalled for potential sterility breaches
Stradis Healthcare is recalling McCormick Medical Distribution PORT TRAY units due to potential pinhole leaks in the outer bag that could compromise sterility. Affected units were distributed nationwide.
Product
McCormick Medical Distribution PORT TRAY, 25 trays per case. Distributed by McCormick Medical Distribution.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0112-2023·2023-01-18
Prostaglandin E1 Injection Vials Recalled for Sterility Issues
Northern VA Compounders PLLC is recalling Prostaglandin E1 Injection Solution vials nationwide due to lack of assurance of sterility. Patients should contact their healthcare provider.
Product
Prostaglandin (E1) Injection Solution, 40mcg/ml, 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0116-2023·2023-01-18
TriMix Injection Recalled Due to Lack of Sterility Assurance
Northern VA Compounders is recalling TriMix Injection due to lack of sterility assurance. The compounded injectable medication may not meet required sterility standards.
Product
TriMix Injection (PGE1/Papaverine HCl/Phentolamine Mesylate) 100mcg/30mg/3mg/mL INJECTABLE, 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0925-2023·2023-01-18
Guarded Luer Connectors Recalled for Compromised Sterility in Blister Packaging
International Medical Industries recalls 228,000 Prep-Fill Guarded Luer Connectors due to unsealed blister packages compromising product sterility. The Class II recall affects medical devices distributed nationwide.
Product
Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400, Female Lock - Female Lock Guarded Luer Connector, Sterile; b. Part number 57-400W, Female Lock - Female Lock Guarded Luer Connector, Sterile; c. Part number 57-401, Female Lock - Male Lock Guarded Luer Co
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0125-2023·2023-01-18
Compounded Injectable Drug Recalled for Lack of Sterility Assurance
Northern VA Compounders PLLC is recalling 1,200 vials of BiMix STD 001 injectable nationwide due to lack of assurance of sterility. The compounded drug cannot be verified as sterile.
Product
BiMix STD 001 (Papaverine HCl/Phentolamine Mesylate) 30mg/1mg/mL INJECTABLE, 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0919-2023·2023-01-18
Anspach Adult Rotating Craniotome Attachment ball bearings may detach during surgery
The Anspach Adult Rotating Craniotome Attachment (CRANI-A-R) may have ball bearings that detach during surgical use. The FDA recommends users follow inspection intervals to prevent potential serious patient injury.
Product
6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-R intended for cutting and shaping bone including the spine and cranium
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0945-2023·2023-01-18
Fluid Filter Transfer Kit Recalled Over Potential Sterility Breaches
Stradis Healthcare is recalling approximately 1,175 Tacy Medical fluid filter transfer kits due to potential pinhole leaks in the outer bag that may compromise sterility. The kits were distributed nationwide in nine states.
Product
Tacy Medical, Inc Fluid Filter Transfer Kit, Sterile, 60 kits per bag, 5 bags per case. Manufactured for Tracy Medical, Inc.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0934-2023·2023-01-18
Henry Shein Sterile Gloves Recalled for Potential Sterility Breach
Stradis Healthcare is recalling Henry Shein sterile gloves due to pinhole leaks in outer packaging that may compromise sterility. The recall affects approximately 21,755 units distributed nationwide.
Product
Henry Shein GLOVES, packaged in the following sizes and descriptions: a. Glove 6.5 Pack, 25 Pairs, 10 packs per case; b. Glove 7.0 Pack, 25 Pairs, 10 packs per case; c. Glove 7.5 Pack, 25 Pairs, 10 packs per case; d. Glove 8.0 Pack, 25 Pairs, 10 packs per case;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0120-2023·2023-01-18
Compounded QuadMix injectable recalled for sterility assurance concerns
Northern VA Compounders PLLC recalled QuadMix Injectable nationwide due to lack of assurance of sterility. Patients who received this compounded medication should contact their healthcare provider immediately.
Product
QuadMix Injectable (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine) 20mcg/20mg/2mg/0.2mg/mL INJECTABLE, 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0924-2023·2023-01-18
Pediatric Craniotome Recalled for Ball Bearing Detachment Risk
The Anspach Effort, Inc. is recalling 6,059 Pediatric Craniotome units (CRANI-P-G1) because ball bearings in the CRANI-A attachment may detach during surgery, potentially causing serious patient injury.
Product
Pediatric Craniotome Ref:CRANI-P-G1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0952-2023·2023-01-18
Medical device software bug may cause patient sample order mismatches in rare cases
A software bug in Roche Diagnostics' cobas infinity central lab may cause orders to be mismatched to wrong patient samples under rare circumstances. The issue affects 224 US units and 2,797 devices worldwide.
Product
cobas infinity central lab, Material Number 07154003001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0916-2023·2023-01-18
Craniotome Attachment Ball Bearings May Detach During Surgery
The Anspach 6.5 cm Adult Rotating Craniotome Attachment may have ball bearings that detach during surgical use or removal. The manufacturer recommends following inspection intervals to prevent serious patient injury.
Product
6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-A Intended for cutting and shaping bone including the spine and cranium
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0910-2023·2023-01-18
Source Administration Set medical device recalled for contamination
The FDA has recalled 2,840 units of the Source Administration Set, a medical device used for PET imaging, due to contamination with black specks on needles.
Product
Source Administration Set (SAS) used with the Medrad Intego PET Infusion System, Sterile Catalog number: INT CSS Affected material number: 86566621 Intended to deliver accurate doses of 18F Fluorodeoxyglucose (FDG) or 18F Sodium Fluoride (NaF) radiopharmaceuticals and commo
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0940-2023·2023-01-18
Central Line Insertion Trays Recalled for Potential Sterility Breaches
Stradis Healthcare is recalling HCT Central Line Insertion Trays due to potential pinhole leaks in the outer bag that may compromise sterility. Approximately 1,176 units were distributed nationwide.
Product
HCT CENTRAL LINE Insertion Tray, I2 per case. Distributed by Health Care Technology
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0909-2023·2023-01-18
Codman Surgical Patties Recalled for Out-of-Specification Endotoxin Levels
Integra LifeSciences is recalling one lot of Codman Surgical Patties due to out-of-specification endotoxin levels. The potential risk is a minor, transient fever.
Product
Codman Surgical Patties, Part number 801400; SURG PATXRAY 1/2X1/2-200; Lot 6396457
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0248-2023·2023-01-18
Sanders Dark Chocolate Sea Salt Caramels Recalled for Foreign Material Contamination
Sanders Candy LLC is recalling its Dark Chocolate Sea Salt Caramels because cleaning brush bristles were found in the product. The affected products were distributed nationwide and in Canada.
Product
Sanders Dark Chocolate Sea Salt Caramels: UPC 0-35900-26442-9 36OZ Tub UPC 0-35900-27488-6 28OZ Tub UPC 0-35900-26442-9 2/36OZ Tub UPC 0-35900-30167-4 7OZ Pouch UPC 0-35900-30852-9 7OZ Gift Box UPC 0-35900-30987-8 18OZ Tub UPC 0-35900-30988-5 9OZ Pouch UPC 0-35900-30969-4 18OZ Tu
Category
Food
Distribution
Distributed nationwide
SevereCPSC·23091·2023-01-12
BISSELL Cordless Wet Dry Vacuums Recalled for Fire Hazard
BISSELL Cordless Multi-Surface Wet Dry Vacuums (models 2551, 2551W, and 25519) are recalled because the battery pack circuit board can overheat and catch fire. The company has received 66 reports of smoking and burning odor, including five fires and one burn injury.
Product
BISSELL® Cordless Multi-Surface Wet Dry Vacuums Models 2551, 2551W and 25519
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·22V921000·2023-01-12
2021 Porsche Taycan Suspension Strut Defect May Cause Loss of Vehicle Control
A retaining ring on the 2021 Porsche Taycan's suspension strut may come loose, causing loss of vehicle control and increasing crash risk. Repairs will be provided free by Porsche dealers.
Product
PORSCHE — 2021 PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V806000·2023-01-12
Freightliner and Mercedes Sprinter paint defect causes window and rail detachment
Daimler Vans USA is recalling Freightliner and Mercedes-Benz Sprinter vans from 2021-2023 due to insufficient paint adhesion that may cause windows and interior lashing rails to detach during a crash. No injuries have been reported.
Product
FREIGHTLINER — 2021 FREIGHTLINER SPRINTER 4500
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23090·2023-01-12
2019-2021 Honda Talon 1000 ROVs Recalled for Engine Failure and Crash Risk
American Honda is expanding its recall of 2019-2021 Honda Talon 1000 recreational off-highway vehicles because a loose intake funnel band screw can enter the engine, cause sudden failure, and result in loss of control and crashes.
Product
2019-2021 Honda Talon 1000 ROVs
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V920000·2023-01-12
2023 Forest River Travel Trailers Recalled for Refrigerator Wiring Fire Risk
Forest River is recalling certain 2023 Wildwood, Salem, and Stealth EVO travel trailers. The 8-gauge refrigerator wire lacks over-current protection, creating a fire risk from melted wiring.
Product
FOREST RIVER — 2023 FOREST RIVER WILDWOOD
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23722·2023-01-12
MI Windows and Doors 1620 Vinyl Single-Hung Impact Windows Recall
MI Windows and Doors is recalling about 25,000 model 1620 vinyl single-hung impact windows with window opening control devices due to a defective tilt latch that can cause the control devices to malfunction, posing fall and serious injury hazards.
Product
1620 vinyl single-hung impact windows with window opening control devices
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V922000·2023-01-12
2023 Jayco Solstice defrost controls may fail, increasing crash risk
Jayco is recalling 2023 Solstice and Entegra Expanse recreational vehicles because the HVAC system's defrost and defog controls may stop working. This loss of visibility control increases the risk of crashes under certain driving conditions.
Product
JAYCO — 2023 JAYCO SOLSTICE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23721·2023-01-12
LG 86-inch Smart Televisions Recalled for Tip-Over and Entrapment Hazards
LG is recalling about 52,000 of its 86-inch smart televisions with stands because the stand can become unstable, creating tip-over and entrapment hazards that can result in injuries or death. Consumers should immediately detach the stands and place the TVs in a safe location away from children.
Product
LG 86-inch smart televisions and stands
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V805000·2023-01-12
Prevost motorcoaches recalled for driver assist sensor obstruction and braking failure risk
Prevost is recalling 2022-2024 H3-45 VIP motorcoaches and 2024 H3-45 models because an incorrect bumper trim panel obstructs the radar sensor, preventing the driver assist system from functioning properly and increasing the risk of crashes.
Product
PREVOST — 2022 PREVOST H3-45 VIP
Category
Vehicle
Distribution
Distributed nationwide