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 48,123 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Feb 12, 2020
Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jjgc Industria E Comercio De Materials Dentarios Sa
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Vaginal Verification Panel Ref 8208 Lot 8208-11
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
ranitidine hydrochloride, USP ,150 mg tablets a) 14-count bottles ( NDC 43063-844-14); b) 30-count bottles (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PD-Rx Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Feb 12, 2020
Ranitidine Hydrochloride (powder), USP, Rx only, Spectrum Chemical Mfg Corp., a) 1 gram, b) 5 grams, c) 25 grams, d)100…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectrum Laboratory Products
FDA (openFDA drug enforcement)
Reported Feb 5, 2020
Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Collagen Matrix Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Ground Ginger in clear plastic bags; Sold in 1 lb. and 5 lb. bags Country of Origin: India 1 lb. UPC: 0 00000 94641 4 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.H.L. Foodservice, Inc. dba H.L. Foods Co.
FDA (openFDA food enforcement)
Reported Feb 5, 2020
CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
21 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Organic IntegriPure Cold Milled Flaxseed, 50 lb Net Wt. and 2000 lb. totes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Healthy Food Ingredients, LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Ingredion ULTRA-TEX4 Food Starch in 50lb paper bags, product code 32166102CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingredion Incorporated
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jeni's Splendid Ice Creams LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kindroot LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McGuff Compounding Pharmacy Services, Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2020
AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Feb 5, 2020
RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Cobas infinity central lab / cobas infinity core license-a Calculator/Data Processing Module, For Clinical Use Material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Frozen Yellowfin Tuna, Product of Vietnam, Packaged under the following brands and cuts: Tidal Seafood Tuna Round…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Truong Phu Xanh Co.,
FDA (openFDA food enforcement)
Reported Jan 29, 2020
TruDi NAV Suction, TDNS000Z, 0 Degree Tip Angle, (01)10705031245877
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2020
Ranitidine, 150 mg Tablets, a) 7 count, b) 14 count, c) 20 count, d) 30 count, e) 60 count; Rx, Only, H.J. Harkins…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.H J Harkins Company Inc. dba Pharma Pac
FDA (openFDA drug enforcement)
Reported Jan 29, 2020
Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paltop Advanced Dental Solutions Ltd.
FDA (openFDA device enforcement)
Reported Jan 29, 2020
Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 150 mg, a) 30 count bottles (NDC: 68788-7388-3), b) 60 count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jan 29, 2020
Ranitidine 150 mg tablet Original Supplier's NDC 65162-0253-10 Remedy Repackaged NDC 70518-1714-00
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug 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.