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.
7,403 stored notices name California, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Nov 6, 2019
Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI :…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
C3 Wave App, v. 2.0.5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk GmbH
FDA (openFDA device enforcement)
Reported Nov 6, 2019
POM Procedural Oxygen Masks, Endoscopic, Conscious Sedation, Bronchoscopy Mask, as follows: (1) POM Medical, LLC, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.POM Medical LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Simmons Prepared Foods, Inc. Retira Productos De Aves Debido A Una Posible Contaminación Con Materia Extraña
High riskUsing this product could cause serious injury, illness or death — stop using it now.Simmons Prepared Foods, Inc.
USDA FSIS
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Jack Daniels Tennessee Whiskey Cake - Chocolate - Net Wt 8 OZ (227 g), UPC: 854621004349
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Great Spirits Baking Company, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 6, 2019
Posey Connected Twice-As-Tough Cuffs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tidi Products
FDA (openFDA device enforcement)
Reported Nov 2, 2019
FSIS Issues Public Health Alert for Raw Pork Products Due to Misbranding and an Undeclared Allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.New York Style Sausage Co.
USDA FSIS
Reported Oct 30, 2019
Ample Hills Peppermint Pattie ice cream packed in 3 gallon tubs and half pint (8oz) cartons . Allergens: Contains:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ample Hills Manufacturing
FDA (openFDA food enforcement)
Reported Oct 30, 2019
Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Andover Healthcare Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Candela Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
MotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CrossRoads Extremity Systems, LLC
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole Packaged Foods, LLC Westlake Village, CA 91361…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dole Packaged Foods, LLC
FDA (openFDA food enforcement)
Reported Oct 30, 2019
Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Oct 30, 2019
ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 30, 2019
The ICS CHARTR EP 200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Irrisept Wound Debridement and Cleansing System. 12 units per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IrriMAX Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 OEM Customer Software: Sentosa SQ Suite Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Holdings Pte Ltd.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
xTAG Respiratory Viral Panel (RVP): Box Label: xTAG RVP (Respiratory Viral Panel). Catalogue Number:I019C0111 in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Molecular Diagnostics
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Roland Foods, LLC
1 more product in this recall
FDA (openFDA food 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.