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 63541–63560 of 68218 results

Sort:

Newest first Oldest first

Elekta, Inc.: Leksell Gamma Knife Perfexion, Article #715000. Telether...

Need to modify the closing speed of the shielding doors in the event of an emergency exit

FDAJul 2, 2007AZ, AR, CA +11 more• Elekta, Inc.

Beckman Coulter Inc: Cytomics FC 500 MPL Flow Cytometry System with MXP Softwa...

Data generation error: If the cytosettings is not refreshed or restarted during data importation, the output will include old and new data.

FDAJun 29, 2007Nationwide• Beckman Coulter Inc

Avazzia, Inc: Avazzia Tennant Biomodulator; Model: BEST AV-1; P/N #TB04...

Plastic Cases may crack due to manufacturing by the supplier not meeting specifications

FDAJun 29, 2007Nationwide• Avazzia, Inc

Avazzia, Inc: Avazzia BEST-RSI; Model: BEST AV-1; P/N #RS04303-103; man...

Plastic Cases may crack due to manufacturing by the supplier not meeting specifications

FDAJun 29, 2007Nationwide• Avazzia, Inc

Vance Products Incorporated: Cook Urological Black Silicone Filiform Double Pigtail Ur...

The radiographic band may detach from the stent and remain in the patient after removal of the stent.

FDAJun 29, 2007Nationwide• Vance Products Incorporated

Avazzia, Inc: Avazzia Med-Best Therapeutic Massager; Model: BEST AV-1; ...

Plastic Cases may crack due to manufacturing by the supplier not meeting specifications

FDAJun 29, 2007Nationwide• Avazzia, Inc

Acumed LLC: Acu-Loc Distal Radius Plate, Standard, Left. Product labe...

Plates are incorrectly laser marked. The PL-DR50L plates are incorrectly laser marked with PL-DR70L.

FDAJun 29, 2007Nationwide• Acumed LLC

Avazzia, Inc: Avazzia Med-Sport Massager; Model: BEST AV-1; P/N #MS0418...

Plastic Cases may crack due to manufacturing by the supplier not meeting specifications

FDAJun 29, 2007Nationwide• Avazzia, Inc

Biomedicare, Inc.: Biomedicare Implantium Fixtures, Model numbers : FX3408, ...

Lack of validation for sterilization cycle: This recall was initiated because the validation of the sterilization process for these devices has not been completed. As a result, Biomedicare cannot assure the sterility of fixtures distributed to date.

FDAJun 29, 2007AZ, CA, IL +3 more• Biomedicare, Inc.

AGFA Corp.: IMPAX 6.2.1 System, Picture Archiving and Communications ...

Text and Images may not be synchronized.

FDAJun 28, 2007Nationwide• AGFA Corp.

Zimmer Inc.: Zimmer Minimally Invasive Solutions Technology, Offset Ra...

Clip Detachment: The retainer c-clip can detach from the instrument during use and may fall into the surgical wound

FDAJun 28, 2007AZ, CA, FL +6 more• Zimmer Inc.

Mini-Mitter Company, Inc.: Actiwatch 64 AM, Bandless Part Number 198-0301-AM1, Respi...

Communication Failure: the devices have a memory chip that has a limited number of read/write cycles which can trigger set up information and/or subject information anomalies or intermittent communication annomalies. If left unaddressed, the issues can lead to permanent communication failure.

FDAJun 27, 2007Nationwide• Mini-Mitter Company, Inc.

Baxa Corporation: Exacta-Mix 2400, OS v1.07, Model No. 8300-0073, Pharmacy ...

A software defect could allow up to 50mL of extra volume being added to a TPN solution.

FDAJun 27, 2007CA, CO, FL +6 more• Baxa Corporation

Mini-Mitter Company, Inc.: Actiwatch 16 Part Number 198-0300-00, Actiwatch 16 AM 198...

Communication Failure: the devices have a memory chip that has a limited number of read/write cycles which can trigger set up information and/or subject information anomalies or intermittent communication annomalies. If left unaddressed, the issues can lead to permanent communication failure.

FDAJun 27, 2007Nationwide• Mini-Mitter Company, Inc.

Mini-Mitter Company, Inc.: Actiwatch 16, Basic Startup pkg 198-1010-00; and Actiwatc...

Communication Failure: the devices have a memory chip that has a limited number of read/write cycles which can trigger set up information and/or subject information anomalies or intermittent communication annomalies. If left unaddressed, the issues can lead to permanent communication failure.

FDAJun 27, 2007Nationwide• Mini-Mitter Company, Inc.

Mini-Mitter Company, Inc.: Actical with Step, Part Number 198-0302-00, Mini Mitter, ...

Communication Failure: the devices have a memory chip that has a limited number of read/write cycles which can trigger set up information and/or subject information anomalies or intermittent communication annomalies. If left unaddressed, the issues can lead to permanent communication failure.

FDAJun 27, 2007Nationwide• Mini-Mitter Company, Inc.

Boston Scientific Corp: Polaris Dx Diagnostic Catheter, for cardiac electrophysio...

Product is mislabeled as hexapolar (6 electrodes), but is actually quadripolar (4 electrodes).

FDAJun 26, 2007FL, IN, TN• Boston Scientific Corp

Carmel Pharma, Inc.: PhaSeal, Protector 14, Item No. P14, US Order No. 21320

Risk of Leakage: When the PhaSeal Protector and Injector are used with drug vials with thick rubber stoppers which have a concave upper surface and a flat bottom surface there is a potential for leakage. These rubber stoppers are made of a harder rubber formulation and may be more difficult to penetrate.

FDAJun 26, 2007Nationwide• Carmel Pharma, Inc.

Carmel Pharma, Inc.: PhaSeal, Protector 50, Item No. 50, US Order No. 10310

Risk of Leakage: When the PhaSeal Protector and Injector are used with drug vials with thick rubber stoppers which have a concave upper surface and a flat bottom surface there is a potential for leakage. These rubber stoppers are made of a harder rubber formulation and may be more difficult to penetrate.

FDAJun 26, 2007Nationwide• Carmel Pharma, Inc.

Arizant Healthcare, Inc: Arizant Healthcare Ranger Standard Flow Blood/Fluid Warm...

Incomplete seal on the product pouch; with the seal incomplete, the sterility of the product inside the pouch cannot be guaranteed.

FDAJun 26, 2007AL, AK, AZ +48 more• Arizant Healthcare, Inc

1...3176 317731783179 3180...3411

Page 3178 of 3411Next