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

Home
/
Brands
/
Nova Biomedical Corporation

Nova Biomedical Corporation Recalls

All product recalls associated with Nova Biomedical Corporation.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

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 6621–6640 of 7756 recalls

Nova Biomedical Corporation: Nova - EZ CHEM Creatinine Meter: SRS Versions 5.1 and 5.2...

Incorrect Results - Creatinine results were lower than the laboratory reference method.

FDANov 2, 2007Nationwide• Nova Biomedical Corporation

Nova Biomedical Corporation: Nova - EZ CHEM Control Solution P/N 9612, Nova Biomedical...

Incorrect Results - Creatinine results were lower than the laboratory reference method.

FDANov 2, 2007Nationwide• Nova Biomedical Corporation

Ski-Doo Snowmobiles (BRP) – Crash and Fire Risk (2007)

Fire/Burn Risk

Ski-Doo Model Year 2008 MXZ Adrenaline 800R, MXZ X 800R, MXZ TNT 500SS, MXZ Trail 500SS, Summit Everest 154 800R snowmobiles are included in this recall. The model name is located on the side panels. They were sold in black/yellow, yellow, or black/slate.

1...330 331332333 334...388

Page 332 of 388Next

CPSCOct 31, 2007Nationwide• Bombardier Recreational Products Inc. (BRP), of Quebec, Canada

B. Braun Interventional Systems: Vena Tech LP Vena Cava Filter System, Item No/REF. 050100...

Sterility (package integrity) compromised: package sealing problem leaving packaging being partially open on one of the four sealed Tyvek pouch edges.

FDAOct 30, 2007Nationwide• B. Braun Interventional Systems

Cardinal Health 303 Inc DBA Alaris Products: Cardinal Health Alaris Pump Module (formerly Medley Pump ...

Inaccurate flow rate; related to misassembled (missing, bent or broken) springs during the manufacturing or servicing of the mechanism assembly

FDAOct 29, 2007AL, AK, AZ +44 more• Cardinal Health 303 Inc DBA Alaris Products

Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila: Abbott TDx/TDxFLx Gentamicin Reagent - Is a reagent for i...

Incorrect Results -- Through evaluation of stability, Abbott have found a decrease in the calibrator A to F span with these reagents lots, which may produce the following results: - Printed Error Code "SPAN LESS THAN MIN SPAN" - Controls out of range. When a control is out of range, patient results should not be reported.

FDAOct 26, 2007AL, AK, AZ +43 more• Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila

Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila: Abbott AxSYM Gentamicin Reagent - Is a reagent for in vit...

FDAOct 26, 2007AL, AK, AZ +43 more• Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila

Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila: Abbott TDx/TDxFLx Gentamicin Wedge Reagent - Is a reagent...

FDAOct 26, 2007AL, AK, AZ +43 more• Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila

Abbott Laboratories, Inc: Abbott, ACCELERATOR Device Manager (ADM); List Number: 08...

Sample/Patient Mis-identification: Two issues identified related to the ACCELERATOR Decision Manager (ADM), to include: 1) Sample Identification (SID) and/or Patient Identification (PID) numbers that contain more than 12 characters are truncated to the final 12 characters by the ADM; 2) for SIDs using alpha characters that are case sensitive, SIDs with lower case characters are transmitted by the

FDAOct 25, 2007Nationwide• Abbott Laboratories, Inc

Concrete Grinders (Blastrac) – Injury Risk (2007)

The recalled gas or electric grinders are used to grind concrete surfaces for repair or removal. The grinders have two wheels, a handle and are blue or green in color. They are designed for operation by a single operator. The following concrete grinders are included in this recall. The serial number is located on a plate on the machine's handle. Blastrac Series BG 250 Concrete Grinders Gas-Powered and Electric-Powered Serial Numbers 26010025 26050053 26060003 26060013 26060014 26070032 26070033 26070034 26070035 26070127 26070131 26080057 26080062 26080085 26100001 26100002 26100003 26100004 26100005 26100006 26100007 26100008 26100009 26100029 26100030 26100031 26100032 26100033 26100034 26100035 26100036 26100037 26100038 26100100 26110058 26110060 26120010 26120011 26120012 26120041 26120042 26120043 26120044 26120045 26120046 26120047 26120048 26120049 26120050 26120051 26120052 26120054 26120055 26120056 26120057 26120058 26120059 26120063 27010006 27010007 27010008 27010009 27010034 27010035 27010036 27010037 27010038 27010039 27010040 27010041 27010042 27010043 27010066 27010067 27010068 27010069 27010070 27020020 27020021 27020060 27020061 27020062 27020063 27020064 27030001 27030002 27030003 27030004 27030005 27030006 27030007 27030060 27030061 27030062 27030063 27030064 27040013 27040014 27040015 27040016 27040017 27040020 27040021 27040046 27040047 27040048 27040049 27040050 27040051 27040052 27040053 27040054 27040055 27040093 27040094 27040095 27040096 27040097 27050023 27050024 27050025 27050026 27050027 27050028 27050029 27050030 27050031 27050032 27050033 27050035 27050036 27050038 27050039 27050040 27050041 27050043 27050046 27050048 27050049 27050050 27050051 27050052 27050063 27050065 27050066 27050067 27050069 27050070 27050071 27050072 27050073 27060014 27060015 27060016 27060017 27060018 27060019 27060020 27060021 27060022 27060023 27060033 27060034 27060035 27060036 27060037 27070013 27070014 27070015 27070016 27070017 27070070 27070099 27070100 27070101 27070102 27080020 27080021 27080022 27080026 27080027 27080042 27080079 27080080 2706009?

CPSCOct 25, 2007Nationwide• Blastrac N.A., of Oklahoma City, Okla.

Baxter Bioscience: Baxter Duploject Easy Prep, Fibrin Sealant Preparation an...

Sterility (package integrity) compromised: This recall is being conducted due to incomplete seal of the product package at the corner of the outer tray and tyvek lid.

FDAOct 25, 2007Nationwide• Baxter Bioscience

Bumbo Baby Sitter Seats (Bumbo) – Head Injury Risk (2007)

The bottom of the children's seat is round and flat with a diameter of about 15 inches. It is constructed of a single piece of molded foam and comes in yellow, blue, purple, pink, aqua, and lime green. The seat has leg holes and seat back that wraps completely around the child. On the front of the seat in raised lettering is the word "Bumbo" with the image of an elephant on top. The bottom of the seat has the following words: "Manufactured by Bumbo South Africa Material: Polyurethane World Patent No. PCT: ZA/1999/00030." The back of the seat contains the following "WARNING" - "Never use on a raised surface. Never use as a car seat or bath seat. Designed for floor level use only. Never leave your baby unattended as the seat is not designed to be totally restrictive and may not prevent release of your baby in the event of vigorous movement."

CPSCOct 25, 2007Nationwide• Bumbo International, of South Africa

Bicycle Forks (Reynolds) – Fall Hazard (2007)

This recall involves the Reynolds UL bicycle fork models with 43 mm and 50 mm rakes and with serial numbers 09100 through 10403. The serial number decal is located on the steer tube. To see the serial number, the fork must be removed from the frame. Some recalled forks are black, have "Reynolds" printed on them, and have a gray and white stripe painted on the legs of the fork. Other recalled forks were painted with a different paint scheme and do not have "Reynolds" printed on them. To determine if a fork is included in this recall, consumers should contact the company.

CPSCOct 23, 2007Nationwide• MacLean Quality Composites, d.b.a. Reynolds, of West Jordan, Utah

Treadmills (Cybex) – Fire Hazard (2007)

Fire/Burn Risk

This recall involves the treadmills "Cybex 400T," "Cybex 410T," "Trotter 510," "Trotter 525", "Trotter 535", and "CXT+" that were recalled on October 8, 2003 and later repaired. The treadmills are black with gray coloring, have rectangular uprights, and measure 69 inches long and 30 inches wide. The brands and models are written on the display panel. The "CXT+" model does not bear the brand Cybex or Trotter.

CPSCOct 23, 2007Nationwide• Cybex International, Inc., of Medway, Mass.

Beckman Coulter Inc: SYNCHRON Systems Salicylate (SALY) Reagent; Part Number: ...

The Salicylate Reagent lots listed here may fail calibration and/or fail to maintain linearity at the upper end of analytical range.

FDAOct 22, 2007Nationwide• Beckman Coulter Inc

Hydration Unit Power Packs (Collegiate Pacific) – Injury Risk (2007)

This recall involves the battery-operated power pack boxes for the 20-gallon "Sports Cool Powered Team Drinker" and the 40-gallon "Sports Cool Powered Tanker with Cart" portable team hydration units. The units include a water tank, six hoses, a battery-operated pack box, and a cart. "Sports Cool" is printed on the water tank.

CPSCOct 22, 2007Nationwide• Collegiate Pacific, of Farmers Branch, Texas

Beckman Coulter Inc: Access Power Supply Assembly Sled Part Number: A48196/684...

Electrical grounding failure: During manufacturing, internal testing found one instrument wlth an intermittent failure of the electrical grounding. The source of the problem was traced to inadequate soldering.

FDAOct 17, 2007Nationwide• Beckman Coulter Inc

Boston Scientific Corporation One Boston: Boston Scientific, Imager II Angiographic Catheter, (Oute...

Mislabeled: Units within the identified lot/batch were incorrectly labeled as 5F on the outer carton and pouch when the product was actually a 4F device.

FDAOct 12, 2007AZ, CA, NJ +1 more• Boston Scientific Corporation One Boston

Abbott Laboratories Inc.: Abbott Clinical Chemistry Creatine Kinase, Model LN 7D63-...

Three potential issues with Creatine Kinase Lot Number: 52044HW00: (1) Decrease in quality control and/or patient results (2) An iIncreased imprecision, or (3) Error Code 1054 (Unable to calculate results, Reaction Failure) on Architect cSystems.

FDAOct 12, 2007Nationwide• Abbott Laboratories Inc.

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with CXP Software V...

Software error: This field action was initiated after Beckman Coulter determined that the CXP software does not refresh the dataset automatically under certain circumstances. The User documentation does not clearly state that the user should refresh the dataset after changes are made.

FDAOct 11, 2007Nationwide• Beckman Coulter Inc