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Recall archive

94,527 stored notices, from Jun 20, 2012 to Oct 2, 2026.

31,892 recalls · page 333 of 1329

Food

Reported Jul 5, 2023

Fanta Orange 12pk (12, 12 oz. cans) Wrap UPC 0 4900003073 0

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

Great Lakes Coca-Cola Distribution LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 5, 2023

Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy samples from soft tissue and tumors of the…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 5, 2023

Kanjo Homeopathic Pain Relief Cream With Arnica, NET WT 2 oz (56.70G), Manufactured For: Acutens, Inc., Sheridan, WY…

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

Homeocare Laboratories, Inc.

10 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Jul 5, 2023

Cinnamon Sticky Buns With Nuts 6 Count Net WT 2 LB 1 OZ (935g). Packaged as a singe pack or 6 pack. Packaged in a…

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

Honest Baking

FDA (openFDA food enforcement)

Medical devices

Reported Jul 5, 2023

LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE; LEGACY SMARTBASE, NE 3.0D 2MML, REF 8730-82NE; LEGACY SMARTBASE NARROW…

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

Implant Direct Sybron Manufacturing LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R

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

Limacorporate S.p.A

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023

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

Luminex Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

Vanta with AdaptiveStim Implantable Neurostimulator, Model 977006; spinal chord stimulation

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery

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

Megadyne Medical Products, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 5, 2023

Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Containers 23.4 oz (666g). Individual units are packaged in…

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

Motts LLP

FDA (openFDA food enforcement)

Medical devices

Reported Jul 5, 2023

PushTracker E2 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P,…

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

Permobil

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) EliA GliadinDP IgG is intended for…

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

Phadia US Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

DigitalDiagnost C90, Model No. 712034 and 712035

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

Immunoassay Premium Level 3-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and…

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

Randox Laboratories Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

Radiation therapy software, RayStation standalone software treatment planning system. Model numbers: 8B, 8B SP1, 8B…

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

RaySearch America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2023

Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm),…

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

Remel, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 5, 2023

Sun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan; Item Number 12151; UPC 715685121512; Net Weight 35.27 oz.…

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

Richin Trading Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 5, 2023

Rudolphs OnYums Onion Flavored Snack Rings 3 oz. UPC 0-24622-57106-9 packaged in metallized film bags, 15 bags per case

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

Rudolph Foods Company

FDA (openFDA food enforcement)

Medical devices

Reported Jul 5, 2023

wDR 2.2 Mobile Digital Diagnostic X-Ray System

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

Sedecal Sa

FDA (openFDA device enforcement)

Food

Reported Jul 5, 2023

Springworks Organic single cut green leaf lettuce, 4 oz.

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

Springworks Farm Inc.

FDA (openFDA food enforcement)

Drugs

Reported Jul 5, 2023

Amphotericin B Liposome for Injection, 50mg/vial, Rx only, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury,…

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

Sun Pharmaceutical Industries Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050

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

Teleflex LLC

122 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jul 5, 2023

Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count Tablets Rx only, Manufactured by: Sun Pharmaceutical…

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

The Harvard Drug Group

FDA (openFDA drug enforcement)

Medical devices

Reported Jul 5, 2023

AEQUALIS FLEX REVIVE Assembly Screw 0mm, Model Number ARS655101

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

Tornier, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

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