Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

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 ↗

Search Product Recalls

Try:····

Filters

Category

All Categories Food Medication Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Time Period

All Time Last 30 Days Last 90 Days Last Year

State

Severity

All Severities Class I (High Risk)Class II (Moderate)Class III (Low)

Source

All Sources FDA CPSC USDA NHTSA

Status

Include terminated recalls

Clear all filters

Showing 22661–22680 of 29086 results

Sort:

Newest first Oldest first

Cypher MIS Screw System (Ebi) – Screw Head Malfunction (2014)

Inoperative screw head seat splay and/or fracture as a result of positioning of the rod which is a part of the Cypher MIS Screw System.

Class IIModerate

FDAOct 8, 2014AL, CA, CT +6 more• Ebi, Llc

Dextroamphetamine Amphetamine (Teva) – Impurity Concern (2014)

Failed Impurities/Degradation Specifications: Out of specification for unknown impurities.

Class IIModerate

FDAOct 8, 2014Nationwide• Teva Pharmaceuticals USA

Cueva Electrode Kit (Ad-Tech) – Applicator Malfunction (2014)

The recall has been initiated due to concerns that the applicator wand may malfunction potentially causing the inability to monitor the VII cranial nerve. .

Class IIModerate

FDAOct 8, 2014Nationwide• Ad-Tech Medical Instrument Corporation

Mortara Surveyor S12 and Surveyor S19 Patient Monitors. ... (Mortara Instrument, Inc) – martara instrument, inc (2014)

Martara Instrument, Inc. has recently became aware of a potential safety hazard involving our Surveyor rand S12 S19 Patient Monitors. A hazardous situation may be created when mounting these monitors using the 75mm VESA mounting hole pattern provided in the battery cover of these monitors. If the mounting screws provided by Mortara are not used and if the mounting screws used are longer than the p

Class IIModerate

FDAOct 7, 2014Nationwide• Mortara Instrument, Inc

RESTORIS PST Acetabular Offset Shell Impactors An impact... (Mako Surgical Corporation) – mako has identified the potential tha... (2014)

MAKO has identified the potential that the shell impactors may be damaged intraoperatively.

Class IIModerate

FDAOct 7, 2014Nationwide• Mako Surgical Corporation

RESTORIS PST Straight Shell Inserter An impactor is a re... (Mako Surgical Corporation) – mako has identified the potential tha... (2014)

MAKO has identified the potential that the shell impactors may be damaged intraoperatively.

Class IIModerate

FDAOct 7, 2014Nationwide• Mako Surgical Corporation

RESTORIS PST Acetabular Straight Shell Impactors An impa... (Mako Surgical Corporation) – mako has identified the potential tha... (2014)

MAKO has identified the potential that the shell impactors may be damaged intraoperatively.

Class IIModerate

FDAOct 7, 2014Nationwide• Mako Surgical Corporation

Bard Dimension Stone Basket Product Usage: The Bard D... (C.R. Bard, Inc.) – the product is non-sterile (2014)

The product is non-sterile.

Class IIModerate

FDAOct 7, 2014AL, FL, IN +7 more• C.R. Bard, Inc.

The Persona Tibial Articular Surface Inserter is a steril... (Zimmer, Inc.) – affected product did not undergo heat... (2014)

Affected product did not undergo heat treatment hardening step leading to the potential for deformation of the tip.

Class IIModerate

FDAOct 7, 2014Nationwide• Zimmer, Inc.

ZEE Aspirin (Zee Medical) – Incorrect Ingredients (2014)

Undeclared Allergen

Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.

Class IIModerate

FDAOct 7, 2014Nationwide• Zee Medical Products Inc

Papaverine HCL Injection (Creative Compounds) – Sterility Risk (2014)

Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Class IIModerate

FDAOct 6, 2014OR, WA• Oregon Compounding Centers, Inc. dba Creative Compounds

Laksell Gamma Knife Perfexion (Elekta, Inc.) – elekta has become aware that the latc... (2014)

Elekta has become aware that the latches may be locked before they have been fully turned resulting in a poorly locked frame.

Class IIModerate

FDAOct 6, 2014Nationwide• Elekta, Inc.

Prednisolone Sodium Phosphate (Creative Compounds) – Sterility Concern (2014)

Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Class IIModerate

FDAOct 6, 2014OR, WA• Oregon Compounding Centers, Inc. dba Creative Compounds

Calcium Chloride Injection (Creative Compounds) – sterility concerns (2014)

Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Class IIModerate

FDAOct 6, 2014OR, WA• Oregon Compounding Centers, Inc. dba Creative Compounds

Sodium Chloride Inhalation (Creative Compounds) – sterility concerns (2014)

Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Class IIModerate

FDAOct 6, 2014OR, WA• Oregon Compounding Centers, Inc. dba Creative Compounds

Jalapeno Albacore Tuna (Bumble Bee) – Pouch seal defect (2014)

Bumble Bee Foods, LLC, has issued a recall on specific codes of pouched Albacore tuna due to defects in the pouch seals which could result in product contamination by spoilage organisms or pathogens, and could lead to illness if consumed.

Class IIModerate

FDAOct 6, 2014Nationwide• Bumble Bee Foods LLC

Estradiol Cypionate (Creative Compounds) – Sterility Concern (2014)

Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Class IIModerate

FDAOct 6, 2014OR, WA• Oregon Compounding Centers, Inc. dba Creative Compounds

Papav HCL/Phentol/Prostaglandin Injectable (Creative Compounds) – Sterility Risk (2014)

Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Class IIModerate

FDAOct 6, 2014OR, WA• Oregon Compounding Centers, Inc. dba Creative Compounds

Prime Fillet Albacore Tuna (Bumble Bee) – Pouch seal defect (2014)

Bumble Bee Foods, LLC, has issued a recall on specific codes of pouched Albacore tuna due to defects in the pouch seals which could result in product contamination by spoilage organisms or pathogens, and could lead to illness if consumed.

Class IIModerate

FDAOct 6, 2014Nationwide• Bumble Bee Foods LLC

Sun Dried Tomato Tuna (Bumble Bee) – Pouch seal defect (2014)

Bumble Bee Foods, LLC, has issued a recall on specific codes of pouched Albacore tuna due to defects in the pouch seals which could result in product contamination by spoilage organisms or pathogens, and could lead to illness if consumed.

Class IIModerate

FDAOct 6, 2014Nationwide• Bumble Bee Foods LLC

1...1132 113311341135 1136...1455

Page 1134 of 1455Next