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 Mar 1, 2023
Nature's Eats Cashew Crave Mix 8 oz. UPC 8-10087-30330-3, packaged in cello bags 12 packages per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Texas Star Nut and Food Co., Inc.
FDA (openFDA food enforcement)
Reported Feb 22, 2023
EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Feb 15, 2023
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
FSIS Issues Public Health Alert for Frozen, Not-Ready-To-Eat Signature Select Breakfast Bowl Products Due to Possible…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Feb 15, 2023
NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
Skinny Dipped Dark Chocolate Cocoa Almonds, 3.5 oz, packaged in flexible plastic pouches inside cardboard cases.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Skinny Dipped
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 15, 2023
Identity Shoulder System Resection Planer 35mm Resection Planer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Conzerol zero molluscum contagiosum, Homeopathic treatment for Molluscum Contagiosum, Topical Cream, Net weight 0.78 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Discovery Pharma LLC
FDA (openFDA drug enforcement)
Reported Feb 8, 2023
FSIS Issues Public Health Alert for Ready-To-Eat Pork Sausage Products Due to Misbranding and an Undeclared Allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Goulart's Sausage Co.
USDA FSIS
Reported Feb 8, 2023
AxiEM" Non-Invasive Patient Tracker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Limited Edition Winter Mint Chocolate Premier Protein 30g Protein High Protein Shake 11.5oz (340mL) UPC 00643843801498…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Niagara Bottling
FDA (openFDA food enforcement)
Reported Feb 8, 2023
Lucid TCD 2.0 System, Model: NA-LUCM1. Transcranial Ultrasound System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NovaSignal Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2023
CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smiths Medical ASD Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2023
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SynCardia Systems LLC
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turbett Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Universal Meditech Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
GORE CARDIOFORM Septal Occluder, REF: GSX0030A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Invisalign Express 10 REF 8512 Invisalign System Comprehensive REF 9000 Invisalign System Moderate REF 9001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Align Technology Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
biokitHSV-2 Rapid Test, REF: 300028001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biokit, S.A.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperVision, Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Future Diagnostics STAT-IntraOperative-Intact-PTH (STAT-IO-I-PTH) Immunoassay kit REF 4K-IPT-00. in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Future Diagnostics Solutions B.V.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Getinge Flow-i Anesthesia Systems Flow-i C20, Part no. 6677200 Flow-i C30, Part no. 6677300 Flow-i C40, Part no. 6677400
High riskUsing this product could cause serious injury, illness or death — stop using it now.Getinge USA Sales Inc.
2 more products in this recall
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.