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Recall archive

94,519 stored notices, from Jun 20, 2012 to Sep 28, 2026.

31,892 recalls · page 255 of 1329

Medical devices

Reported May 1, 2024

Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion…

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

Ebi, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog Number: EG-1000 Software Version: N/A Product…

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

Electro Medical Systems SA

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported May 1, 2024

Cloderm (clocortolone pivalate) Cream, 0.1%, Rx Only, For Topical Use Only, Net Wt 45g, Manufactured for: EPI Health,…

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

EPI Health, LLC

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2024

ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.

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

FA Online Inc.

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2024

Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only,…

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

Glenmark Pharmaceuticals Inc., USA

FDA (openFDA drug enforcement)

Food

Reported May 1, 2024

Kowalski Simply Sides - Jack's Potato Salad, 16oz. plastic tub, UPC: 754721282701. 6 retail tubs per wholesale case.

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

Home Style Foods, Inc.

FDA (openFDA food enforcement)

Drugs

Reported May 1, 2024

Eyesaline, Saline Eyewash Solution, Cartridge for Fendall 2000, Net contents: 7.9 gal per cartridge, Sperian Eye & Face…

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

Honeywell Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 1, 2024

TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog…

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

Howmedica Osteonics Corp.

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

IBA Proton Therapy System - PROTEUS 235, PTS-10 versions, PTS-11 versions, and PTS-12 versions.

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

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Leica HistoCore PEGASUS (PROCESSOR, TISSUE, AUTOMATED)

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

Leica Biosystems Nussloch GmbH

FDA (openFDA device enforcement)

Drugs

Reported May 1, 2024

GloStrips, Fluorescein Sodium Ophthalmic Strips USP (0.6 mg Fluorescein), Rx Only, a) 100 strips per carton, NDC…

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

Nomax Inc.

3 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported May 1, 2024

Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

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

Parker Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported May 1, 2024

12 oz Aluminum cans of root beer packaged 12 cans per carton. 2/12pks per case

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

Pepsico Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 1, 2024

Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT…

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

Philips North America LLC

FDA (openFDA device enforcement)

Drugs

Reported May 1, 2024

Spanish Fly 22K capsules, 2-count box, UPC 0 664979 979455

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

Pyramids Wholesale Inc.

10 more products in this recall

FDA (openFDA drug enforcement)

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)

Food

Reported May 1, 2024

Roly Poly Bakery brand MULTIGRAIN bread; INGREDIENTS: Whole Wheat Flour, High Gluten Flour, Ryechops, Sesame, Caraway,…

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

Roly-Poly Bakery

FDA (openFDA food 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

Mariner RDX Polyaxial Head, REF: MX1-000020; Mariner RDX Extended Polyaxial Head, REF: MX1-000030; Mariner RDX…

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

Seaspine Orthopedics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported May 1, 2024

Abilify (aripiprazole), 5 mg tablets, packaged in 30 count bottles, RX only, Otsuka America Pharmaceutical, Inc., NDC…

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

Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

3 more products in this recall

FDA (openFDA drug 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)

Food

Reported May 1, 2024

Ready Meals Teriyaki Salmon W Rice 13.5OZ TRAY BLK&GOLD ALUM 22OZ with Plastic Lid #81061425 UPC: 002113010092 Sell…

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

Taylor Farms Southwest, Inc.

FDA (openFDA food 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)

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