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Revive Rx LLC dba Revive Rx Pharmacy

Revive Rx LLC dba Revive Rx Pharmacy Recalls

All product recalls associated with Revive Rx LLC dba Revive Rx Pharmacy.

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Recall Summary

Total Recalls

1000

Past Year

896

Class I (Serious)

125

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1541–1560 of 17592 recalls

Tirzepatide (Revive Rx) – Labeling Mix-up (2024)

Labeling: Label Mix-up - product labeled as tirzepatide contains testosterone cypionate

Class IHigh

FDAApr 20, 2024Nationwide• Revive Rx LLC dba Revive Rx Pharmacy

Coachmen Catalina (Coachmen) – appliance panel problem (2024)

Fire/Burn Risk

Forest River, Inc. (Forest River) is recalling certain 2024 Coachmen Catalina BCAT154RDX and Forest River Aurora BART15RDX travel trailers. The panel that isolates the cooktop from the furnace was not properly sealed during manufacturing, which could result in an inverted cooktop flame.

High

NHTSAApr 19, 2024Nationwide• COACHMEN

Primal Kitchen Avocado Oil (Kraft Heinz) – Bottle Breakage (2024)

The product's glass bottle may be prone to breakage

1...76 777879 80...880

Page 78 of 880Next

Class IIModerate

FDAApr 19, 2024AZ, CA, GA +7 more• KRAFT HEINZ FOODS COMPANY

DxI 9000 Access Immunoassay Analyzer (Beckman Coulter) – diagnostic device issue (2024)

Beckman Coulter is recalling their DxI 9000 Access Immunoassay Analyzers, an in vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids, by correction. The reason for the recall is: Beckman Coulter has determined that the DxI 9000 Access Immunoassay analyzer accepts calibrator values scanned from multiple calibrator cards when an operator configures a new calibrator lot. The analyzer accepts the calibrator lot values from any scanned calibrator card, regardless of the assay test code or calibrator material lot number. The software is not validating the integrity of each calibrator barcode scanned to ensure they are all from the same calibrator card. This includes all software versions and all DxI 9000 instruments that are currently in the field. This issue does not impact calibrator material with 2D calibrator card barcodes. This may cause a failed calibration curve. The health risk to patients is dependent upon the analytes that could be impacted by the error, to include receiving delayed or erroneous results. The issue was identified by Beckman Coulter while conducting a field action on DxI 9000 Access Immunoassay Analyzers.

High

FDAApr 18, 2024Nationwide• Beckman Coulter, Inc.

Vercise Genus DBS Implantable Pulse Generator (Boston Scientific) – system check issue (2024)

Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset. The device reset could lead transient loss of stimulation; patients may experience undesired sensations, transient worsening of movement disorder symptoms, which may lead patient to request surgical intervention for replacement or revision.

High

FDAApr 18, 2024Nationwide• Boston Scientific Neuromodulation Corporation

Mi1250 SYNCHRONY 2 (MED-EL) – internal electronics crack (2024)

A small number of devices may have a higher probability of a crack within the internal electronics substrate which could result in a non-functional device.

Moderate

FDAApr 18, 2024NC• MED-EL Elektromedizinische Gereate, Gmbh Furstenweg 77a Innsbruck Austria

Beckman Coulter DxL 9000 Analyzer (Beckman Coulter) – calibration request problem (2024)

When the DxI 9000 Access Immunoassay Analyzer with system software version 1.16.2 and prior is configured to automatically request a calibration order, the instrument can process the order with expired calibrator material. If the calibration curve is generated with an expired calibration material lot, this may lead to a hazardous situation of erroneously high or low patient results reported to the physicians.

High

FDAApr 18, 2024FL, GA, IN +6 more• Beckman Coulter, Inc.

OES 4000 Hysteroscope (Olympus) – leakage test omission (2024)

The required leakage test was not performed following of a re-work for a non-conformity. This could potentially result in liquid ingress into the eyepiece and cause a foggy image.

Low

FDAApr 18, 2024Nationwide• Olympus Corporation of the Americas

Tiramisu Dessert (Mama Mucci's) – Undeclared Milk (2024)

Undeclared Milk

Undeclared milk and incomplete Contains statement

Class IIModerate

FDAApr 18, 2024MI• Mucci Food Products, Ltd. DBA Mama Mucci's Pasta

Goat Milk Toddler Formula (Sammy's Milk) – Marketing Issue (2024)

FDA inspection and investigation of firm's website and social media pages found that Sammy's online marketing materials included misleading information that implied the product was safe as a sole source of nutrition for infants. Sammy's Milk has not submitted to FDA the premarket notification required for an infant formula, and the product is not manufactured in compliance with the infant formula requirements.

Class IHigh

FDAApr 18, 2024AL, AK, AZ +40 more• Graceleigh, Inc. dba Sammy's Milk

Goat Milk Toddler Formula (Sammy's Milk) – Marketing Issue (2024)

FDA inspection and investigation of firm's website and social media pages found that Sammy's online marketing materials included misleading information that implied the product was safe for use as a sole source of nutrition for infants. Sammy's Milk has not submitted to FDA the premarket notification required for an infant formula, and the product is not manufactured in compliance with the infant formula requirements.

Class IHigh

FDAApr 18, 2024AL, AK, AZ +40 more• Graceleigh, Inc. dba Sammy's Milk

Mocha Hazelnut Wafer (Sacramento Cookie) – Undeclared Milk (2024)

Undeclared Allergen

Undeclared allergen (milk)

Class IIModerate

FDAApr 17, 2024AL, AK, AZ +12 more• Sacramento Cookie Factory

Raspberry Almond Wafer (Sacramento Cookie) – Undeclared Milk (2024)

Undeclared Allergen

Undeclared allergen (milk)

Class IIModerate

FDAApr 17, 2024AL, AK, AZ +12 more• Sacramento Cookie Factory

Vanilla Almond Wafer (Sacramento Cookie) – Undeclared Milk (2024)

Undeclared Allergen

Undeclared allergen (milk)

Class IIModerate

FDAApr 17, 2024AL, AK, AZ +12 more• Sacramento Cookie Factory

Wine Wafer (Sacramento Cookie) – Undeclared Milk (2024)

Undeclared Allergen

Undeclared allergen (milk)

Class IIModerate

FDAApr 17, 2024AL, AK, AZ +12 more• Sacramento Cookie Factory

Original Wine Wafer - Lemon Vanilla (Sacramento Cookie Factory) – Undeclared Milk (2024)

Undeclared Allergen

Undeclared allergen (milk)

Class IIModerate

FDAApr 17, 2024AL, AK, AZ +12 more• Sacramento Cookie Factory

Gold Medal Apple Juice (Martinelli's) – Elevated Arsenic Levels (2024)

Elevated levels of inorganic arsenic.

Class IIModerate

FDAApr 16, 2024AL, AZ, AR +32 more• S Martinelli & Company

CARDIOHELP-i System (Maquet) – patient leakage current (2024)

The firm identified that the measured patient leakage current in some devices significantly exceeded expected levels.

High

FDAApr 15, 2024Nationwide• Maquet Medical Systems USA

MyoSPECT System (GE Medical) – lead cover handle risk (2024)

There is a potential issue regarding the service handles for the internal lead (Pb) covers in that the handles could loosen or release which could cause a cover to drop potentially resulting in injury to service personnel due to the weight of the cover.

Moderate

FDAApr 15, 2024Nationwide• GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING 4, Hayozma St Tirat Carmel Israel

Dairy Products (Hiland Dairy) – Potable Water Issue (2024)

May contain potable water.

Class IIILow

FDAApr 12, 2024KS, MO• Hiland Dairy Foods Company, LLC