Recalls distributed in California
These notices name California in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
7,507 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Oct 18, 2023
LittleOak Natural Goat Milk Infant Formula (Stage 1); packaged in 800g (1.8lbs) tin cans - six cans per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Little Oak Company Ltd.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 11, 2023
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Puritan Bennett Cuff Pressure Manager, REF: 180-03
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Oct 11, 2023
therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used on the Rotor-Gene Q MDx instrument for the detection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen GmbH
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Heartmate 3 LVAS Implant Kit, REF: 106524US, 106524INT; Heartmate XVE & HeartMate II Apical Coring Knife, REF: 1050
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT; Total package size: 12 bottles per case;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vive Organic
FDA (openFDA food enforcement)
Reported Oct 6, 2023
FSIS Issues Public Health Alert for Kirkland Signature Ready-To-Eat Ham Products Due to Possible Listeria Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.JBS Prepared Foods, Inc.
USDA FSIS
Reported Oct 4, 2023
Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 4, 2023
1 lb. bags of CellarScience ascorbic acid, packaged in vinyl bags on 11/18/2022, Sku: AD615LB, Batch Number 56559, UPC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Moreflavor, Inc.
FDA (openFDA food enforcement)
Reported Oct 4, 2023
Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part Numbers 1053617 (US) and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
FDA (openFDA device enforcement)
Reported Oct 4, 2023
Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Sep 27, 2023
COOLIEF RF Generator is an 80-watt Radio-Frequency (RF) Generator with four independent RF channels, allowing all RF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Perifix¿ / Epidural anesthesia set, medicated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Copan Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
DJO Surgical: Empowr Knee, Universal Tibia Baseplate, 6R, REF: 352-02-106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with CardioLab AltiX and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Cheese Spread Pasteurized Process packaged under the following brands and sizes: 1. bowl & Basket, A Shoprite Brand,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Great Lakes Cheese, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2023
Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, REF 71421265; knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Welch Allyn Connex Spot Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Sep 20, 2023
FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new California recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.