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 Aug 3, 2022
Just Egg Spring Greens Broccoli, Peas, Spinach, Kale, Basil, Dill Chopped plant egg NET WT 12 OZ (340g) UPC 1 91011…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eat Just Inc.
FDA (openFDA food enforcement)
Reported Aug 3, 2022
Juice Beauty, The Organic Solution, SPF 8, Joyful Lip Moisturizer, Hydratant pour les Levres, NET WT 0.15 oz (4.25 g)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Eco Lips, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 3, 2022
Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Sight OLO, Automated Hematology Analyzer, Catalog No. OLO-U1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sight Diagnostics Ltd.
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Stryker 2.3mm Tapered Router, Catalog no. 5820-071-023 instrument used in craniotomy procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments
FDA (openFDA device enforcement)
Reported Aug 3, 2022
etouchus, model no. ETM-G01. Noninvasive Blood glucose meter.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Touch US LLC
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Nifedipine WSP 0.2% Ointment, 60 gram tubes, Rx only, Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704
High riskUsing this product could cause serious injury, illness or death — stop using it now.Valor Compounding Pharmacy, Inc. dba Valor Compounding Pharmacy
FDA (openFDA drug enforcement)
Reported Jul 27, 2022
ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Panera Bread at Home Southwest Corn Chowder, 16 oz. (453 g)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blount Fine Foods Corporation
FDA (openFDA food enforcement)
Reported Jul 27, 2022
GreenLight HPSEA Laser Fibers, UPN 0010-2092
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Item 38180-12, Chuckanut Bay Cheesecake Bites New York + Chocolate. Perishable - Keep Refrigerated. There are 8 pieces…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chuckanut Bay Foods LLC
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2022
LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
LumiraDx SARS-CoV-2 Antibody (Ab) Test Strip
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LumiraDx
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Lemon Muffins, item # 802387, are packaged in paper tray and covered with plastic film shrink wrap. Each tray contains…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Portland Specialty Baking LLC
FDA (openFDA food enforcement)
Reported Jul 27, 2022
Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.R & D Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Revie Superfoods Berry Blu 194g Ready-to-Blend Blueberry Creamsicle Smoothie Made in Canada UPC 8 54681 00005 3 Revive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Revive Organics, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2022
(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
SX-One MicroKnife
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonex Health LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jul 27, 2022
NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Synapse Biomedical Inc.
FDA (openFDA device enforcement)
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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.