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 48,100 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported May 1, 2024

QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests

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

Quidel Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Route 92 Medical Full Length 070 Access System, REF 7002, Rxonly, SterileEO. Used for Introduction of interventional…

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

Route 92 Medical Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System,…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the…

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

XENEX Disinfection Services Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 24, 2024

Abdallah Sea Salt Almond Alligators. Net Weight 8 ounces (226g). UPC 7 66684-00412 2. Abdallah Candies, Made in Apple…

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

Abdallah Incorporated

FDA (openFDA food enforcement)

Food

Reported Apr 24, 2024

Aromitalia Malasia Coconut Paste + 35.27 oz milk-based mix, Net Weight 123.46 oz, plastic container.

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

Aromitalia USA Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 24, 2024

Tranquility & Teachings William Monague plate set, brand Indigenous Collection by CAP. Each box consists of two plates,…

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

Canadian Art Prints

FDA (openFDA food enforcement)

Meat & poultry

Reported Apr 24, 2024

ConSup North America Inc. Recalls Ready-To-Eat Sliced Prosciutto Product Produced Without Benefit of Inspection

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

ConSup North America Inc.

USDA FSIS

Medical devices

Reported Apr 24, 2024

Chiba Biopsy Needle - Used for aspiration biopsy. REFERENCE PART NUMBER (RPN) ORDER NUMBER (GPN): 1) DCHN-18-10.0…

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

Cook Incorporated

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 24, 2024

MK Cinnamon Powder, 45g, plastic bottle

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

Mak Trading Co. Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 24, 2024

Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor), REF:9210, Rx Only,

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

Masimo Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

Tablo Hemodialysis System, REF: PN-0003000, PN-0006000 and PN-0007001

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

Aeris EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)

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

Philips Respironics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.

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

SonarMed Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

POLYSIN (Polyglycolic Acid) suture, HSM9 5-0 BR PGA Part Number G503N

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

Surgical Specialties

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2024

ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1…

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2024

LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0.

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

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2024

Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient…

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

Human Care Hc Sweden Ab

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2024

Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2024

KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b, a) REF 0209P and b) REF 0209K, Quality control kit for…

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 17, 2024

Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Electrolytic tin-plated cans, with paper label. 12-pack case…

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

Whitley Peanut Factory, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 10, 2024

3M Tube Securement Device, Small, 1.7 IN/PO x 2.4 IN/PO, REF 1500U, Sterile; and 3M Tube Securement Device, Large, 2.2…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Apr 10, 2024

ARCHITECT STAT Myoglobin Reagent Kit, LN 2K43-25 and 2K43-20.

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

Abbott Laboratories

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.