All recall categories

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.

Drugs

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

Reported Jul 27, 2022

X80 RADiant Photoelectric Therapy System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Xstrahl Limited

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Alcon Custom Pak Surgical Procedure Pack: 16998-11 2519351H SALAHUDDIN 2.4 PACK FRESNO SURGICAL HOSP 18392-03 14HDFF…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cordis US Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

HAMILTON-H900 Humidifier, Models: 950001, 950004

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2022

Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a purple bag and an inside silver flexible…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

J & M Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 20, 2022

Market Day Krabbycakes, Item 3320, Net Wt. 40 oz. (2.5 lbs.) 1.13kg. Item Number 803320R. UPC 51497 14360. Light panko…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Market Day Local Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 20, 2022

MiniMed 620G Insulin Pump (O.U.S. version)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed

7 more products in this recall

FDA (openFDA device enforcement)

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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.