Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Search Product Recalls

Try:····

Filters

Time Period

All Time Last 30 Days Last 90 Days Last Year

State

Showing 22981–23000 of 29086 results

Sort:

Newest first Oldest first

Pre-Cooked Scrambled Eggs (Papetti's) – spoilage risk (2014)

Product may be contaminated with spoilage microorganism.

Class IIModerate

FDAAug 29, 2014Nationwide• Michael Foods, Inc.

Pre-Cooked Scrambled Eggs (Papetti's) – spoilage risk (2014)

Product may be contaminated with spoilage microorganism.

Class IIModerate

FDAAug 29, 2014Nationwide• Michael Foods, Inc.

Chocolate Caramel Balls (R.M. Palmer) – undeclared peanut (2014)

Undeclared Nuts

Product contains undeclared peanut butter. Peanut butter coated chocolate balls packed in bags labeled as Creepy Peepers Chocolaty Coated Soft Caramel Filled Eyeballs

Class IIModerate

FDAAug 29, 2014AL, FL, HI +5 more• R.M. Palmer Company

Dimension Vista CKMB Calibrator (Siemens) – Calibration Drift (2014)

Siemens Healthcare Diagnostics has determined that Dimension Vista® Mass CKMB Isoenzyme Calibrator (MMB CAL) shows drift during routine stability monitoring that exceeds our acceptance criteria for drift over the shelf life of this product. Siemens has observed drift from 3% to 12% at MMB concentrations across the assay range. Depending on quality control limits, this drift may not have been d

Class IIModerate

FDAAug 28, 2014Nationwide• Siemens Healthcare Diagnostics, Inc.

Powdered Donettes (Hostess) – mold growth risk (2014)

Products recalled due to potential for mold growth. Laboratory analysis for products manufactured demonstrated a higher-than-average moisture content.

Class IIModerate

FDAAug 28, 2014Nationwide• Hostess Brands LLC

Powdered Donettes (Hostess) – frozen mold risk (2014)

Products recalled due to potential for mold growth. Laboratory analysis for products manufactured demonstrated a higher-than-average moisture content.

Class IIModerate

FDAAug 28, 2014Nationwide• Hostess Brands LLC

Frosted Donettes (Hostess) – frozen mold risk (2014)

Products recalled due to potential for mold growth. Laboratory analysis for products manufactured demonstrated a higher-than-average moisture content.

Class IIModerate

FDAAug 28, 2014Nationwide• Hostess Brands LLC

Hostess Powdered Donettes (Hostess) – mold growth risk (2014)

Products recalled due to potential for mold growth. Laboratory analysis for products manufactured demonstrated a higher-than-average moisture content.

Class IIModerate

FDAAug 28, 2014Nationwide• Hostess Brands LLC

TRx Vertical Positioner (Motion Concepts) – Knee Support Failure (2014)

Motion Concepts identified that there is a possibility of knee support failure occurring through fatigue of two attachment bolts in the Vertical Position System (TRx Vertical Positioner).

Class IIModerate

FDAAug 28, 2014AR, CA, CT +15 more• Motion Concepts

Hostess Frosted Donettes (Hostess) – mold growth risk (2014)

Products recalled due to potential for mold growth. Laboratory analysis for products manufactured demonstrated a higher-than-average moisture content.

Class IIModerate

FDAAug 28, 2014Nationwide• Hostess Brands LLC

Oxycodone-Acetaminophen Tablets (Alvogen) – Dosage Uniformity Issue (2014)

Failed Content Uniformity Specifications - The lot failed to meet the acceptance criteria for Uniformity of Dosage Units at the time of release for the oxycodone component.

Class IIModerate

FDAAug 28, 2014Nationwide• Alvogen, Inc

Dermatend Original (Solace International) – Unapproved Claims (2014)

Labeling: Labeling Bears Unapproved Claims; Dermatend is not FDA approved and therefore has not been shown to be safe and effective for the uses suggested in the labeling.

Class IIModerate

FDAAug 28, 2014Nationwide• Solace International Inc

Dermatend Ultra (Solace International) – Unapproved Claims (2014)

Labeling: Labeling Bears Unapproved Claims; Dermatend is not FDA approved and therefore has not been shown to be safe and effective for the uses suggested in the labeling.

Class IIModerate

FDAAug 28, 2014Nationwide• Solace International Inc

Hostess Powdered Donettes (Hostess) – mold growth risk (2014)

Products recalled due to potential for mold growth. Laboratory analysis for products manufactured demonstrated a higher-than-average moisture content.

Class IIModerate

FDAAug 28, 2014Nationwide• Hostess Brands LLC

Bionector Connector (Vygon) – Membrane Elasticity Problem (2014)

Vygon has uncovered potential problems with membrane elasticity in the 896.038, Bionector Needleless connector and is issuing a voluntary recall of the 896.038, Bionector Needleless connector.

Class IIModerate

FDAAug 28, 2014CA• Vygon Corporation

Fluocinonide Gel (Fougera) – Stability Specification Failure (2014)

Failed Stability Specifications: The lots of Fluocinonide Gel USP, 0.05% recalled, may not meet the requirements for residual solvents as outlined in USP <467>.

Class IIModerate

FDAAug 28, 2014Nationwide• Fougera Pharmaceuticals Inc.

eFilm Workstation (Merge Healthcare) – Software Thumbnail Issue (2014)

There is an issue related to eFilm Workstation versions 4.0 and 4.0.1 when having multiple studies open and utilizing the thumbnail panel to select multiple series from multiple studies may lead to the selection of an incorrect study.

Class IIModerate

FDAAug 28, 2014Nationwide• Merge Healthcare, Inc.

JustRight 5mm Reload (Justright Surgical) – Staple Formation Risk (2014)

Laceration Risk

JustRight Surgical is recalling specific lots of JustRight 5mm Stapler and Reload products because they may deliver poor distal staple formation, past the end of the knife cut.

Class IIModerate

FDAAug 27, 2014CA, CO, IN +1 more• Justright Surgical, LLC

Testosterone Cypionate Injectable (Martin Avenue) – sterility concern (2014)

Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.

Class IIModerate

FDAAug 27, 2014Nationwide• Martin Avenue Pharmacy, Inc.

Lidocaine Injectable (Martin Avenue) – sterility concern (2014)

Class IIModerate

FDAAug 27, 2014Nationwide• Martin Avenue Pharmacy, Inc.

1...1148 114911501151 1152...1455

Page 1150 of 1455Next