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Nova Biomedical Corporation

Nova Biomedical Corporation Recalls

All product recalls associated with Nova Biomedical Corporation.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

25

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 6981–7000 of 7756 recalls

Nova Biomedical Corporation: Stat Profile Critical Care (CCX) Analyzer Catalog Number...

Analyzers may fail to perform scheduled automatic two-point calibrations and Quality Control runs

FDAJan 27, 2006Nationwide• Nova Biomedical Corporation

Nova Biomedical Corporation: Stat Profile Critical Care PLUS (CCX) Analyzer Catalog ...

Analyzers may fail to perform scheduled automatic two-point calibrations and Quality Control runs

FDAJan 27, 2006Nationwide• Nova Biomedical Corporation

Nova Biomedical Corporation: CCX Operating Software , Version 4.08

Analyzers may fail to perform scheduled automatic two-point calibrations and Quality Control runs

FDAJan 27, 2006Nationwide

1...348 349350351 352...388

Page 350 of 388Next

• Nova Biomedical Corporation

RC2 Brands Inc., The First Years: The First Years Cool Animal Teether/Fish, Zebra and Dinos...

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

RC2 Brands Inc., The First Years: Disney Baby Soft Cool Ring Teether Style # Y1470

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

RC2 Brands Inc., The First Years: Sesame Beginnings Chill & Chew Teether Style #Y3095

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

RC2 Brands Inc., The First Years: The First Years Floating Friend Teether Style #Y1474

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

RC2 Brands Inc., The First Years: Disney Days Hunny Cool Ring Teether Style # Y1447

Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

FDAJan 25, 2006Nationwide• RC2 Brands Inc., The First Years

Porter-Cable 890 Series Routers – Repair Needed (2006)

Laceration Risk

The recalled Porter-Cable routers are tools used in conjunction with various bits to cut and shape wood. The model and serial numbers are printed on the nameplate on the top of the router. Routers marked with a "T" above "PORTER+CABLE" on the nameplate are not included in this recall. Model Number Porter-Cable Product Name Serial Number 891 2 ¼ Peak HP Gripvac™ Router 10001 through 24647 892 2 ¼ Peak HP Router Kit 10001 through 68442 893PK 2 ¼ Peak HP Multibase Router Kit 10001 through 68442 894PK 2 ¼ Peak HP Multibase Router Kit with Gripvac™ Attachment 10001 through 24647 895PK 2 ¼ Peak MP Multibase Router Kit with Router Table Height Adjuster 10001 through 68442 8902 2 ¼ Peak HP Variable-Speed Motor 10001 through 68442

CPSCJan 24, 2006Nationwide• Porter-Cable, of Jackson, Tenn.

Bayer Healthcare, LLC (Diagnostics Division): Brand Name: RapidLab 1200 System, Model 1240, Part Number...

When stored data is recalled from memory, the results do not agree with the original results. Software anomaly: a calculation error occurs when using the correlation adjustment feature on the RapidLab 1200 Systems with software versions 1.0, 1.01, or 1.02. The correlation feature applies user-defined slope and offset parameters each time stored test results are recalled to the display.

FDAJan 20, 2006Nationwide• Bayer Healthcare, LLC (Diagnostics Division)

Thera Test Laboratories, Inc.: EL-aCL Anti-Cardiolipin ELISA Kit; an in-vitro diagnostic...

The specimen diluent contained in the kits was contaminated with a fungal growth. Also, a portion of kit lot 09055514 was shipped without the Data Sheet, part #201-204.

FDAJan 11, 2006CA, CT, FL +4 more• Thera Test Laboratories, Inc.

Baxter Healthcare Corp. Rt.: Baxter Epidural Anesthesia Trays that contain BD Catheter...

The BD catheter connector contained in the Epidural Anesthesia Trays may not fully secure the catheter and allows the catheter to either become loose or disconnected from the connector.

FDAJan 10, 2006Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Continuous Epidural Anesthesia Trays that contain ...

The BD catheter connector contained in the Epidural Anesthesia Trays may not fully secure the catheter and allows the catheter to either become loose or disconnected from the connector.

FDAJan 10, 2006Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Combined Epidural Anesthesia Trays that contain BD...

The BD catheter connector contained in the Epidural Anesthesia Trays may not fully secure the catheter and allows the catheter to either become loose or disconnected from the connector.

FDAJan 10, 2006Nationwide• Baxter Healthcare Corp. Rt.

Ski-Doo Snowmobiles (Bombardier) – Additional Model Defect (2006)

The recall involves certain Ski-Doo Model Year 2006 REV500 SS, REV 600 HO, and REV 600 HO SDI snowmobiles. For a complete list of model numbers and serial numbers affected by this recall please log onto www.ski-doo.com The model number and serial number can be found on the tunnel. Year Model Package Model Number 2006 MX Z Adrenaline 000BE6C00 000BE6D00 000BE6E00 000BE6F00 000BF6C00 000BF6D00 2006 MX Z Trail 000BH6B00 2006 MX Z Renegade X 000BW6C00 2006 GSX Sport 000DC6A00 000DC6B00 2006 GTX Sport 000ED6A00 000ED6B00 000ED6C00 000EJ6A00 000EJ6B00 2006 GTX Ltd 000EH6B00

CPSCJan 5, 2006Nationwide• Bombardier Recreational Products Inc., of Valcourt, Quebec

Ski-Doo Snowmobiles (Bombardier) – Vehicle Safety Concern (2006)

The recall involves certain Ski-Doo Model Year 2006 snowmobiles. The platforms involved are the REV, RT, and RF. For a complete list of model numbers and serial numbers affected by this recall please log onto www.ski-doo.com Check the owner's manual for the location of the model number and serial number. Most are located on the tunnel. Year Model Package Model Number 2006 MX Z Adrenaline 000BD6A00 000BD6B00 000BD6C00 000BD6D00 000BD6E00 000BD6F00 000BE6A00 000BE6B00 000BE6C00 000BE6D00 000BE6E00 000BE6F00 000BF6A00 000BF6B00 000BF6C00 000BF6D00 000BL6A00 000BL6B00 000BL6C00 000BL6D00 000BL6E00 000BL6F00 2006 MX Z Trail 000BH6A00 000BH6B00 000BH6C00 2006 MX Z Fan 000BP6A00 000BR6A00 000BR6B00 2006 MX Z Renegade 000BU6A00 000BU6B00 000BU6C00 000BU6D00 000BX6A00 000BX6B00 000BX6C00 000BX6D00 2006 Summit Highmark 000CD6A00 000CD6B00 000CE6A00 000CE6B00 000CE6C00 2006 Summit Adrenaline 000CJ6A00 000CJ6B00 000CJ6C00 000CK6A00 000CK6B00 000CL6A00 000CL6B00 000CL6C00 2006 Summit Fan 000CM6A00 000CM6B00 2006 GSX Ltd 000DA6A00 000DA6B00 000DD6A00 000DD6B00 2006 GSX Sport 000DC6A00 000DC6B00 000DE6A00 000DE6B00 2006 GSX Fan 000DF6A00 000DG6A00 2006 GTX Ltd 000EA6A00 000EA6C00 000EH6A00 2006 GTX Sport 000ED6A00 000ED6B00 000ED6C00 000EJ6A00 000EJ6B00 000EJ6C00 2006 GTX Fan 000EL6A00 000EL6B00 000EL6C00 000EM6A00 000EM6B00 000EM6C00 2006 Expedition Sport 000EN6A00 000EN6B00 2006 Skandic Tundra 000GA6A00 000GA6B00 000GA6C00 2006 Freestyle Freestyle 000GB6A00 000GB6B00 000GB6D00 000GB6E00 000GB6F00

CPSCJan 5, 2006Nationwide• Bombardier Recreational Products Inc., of Valcourt, Quebec

BioHorizons Implant Systems Inc One Perimeter Park South: BioHorizons Maximus 3.0 surgical kit, also marketed as Bi...

Dental implants were distributed which lacked the proper instruments for implantation.

FDADec 28, 2005Nationwide• BioHorizons Implant Systems Inc One Perimeter Park South

Blackstone Medical Inc.: ICON Modular Spinal Fixation System used with the: ICON I...

Pedicle Screw may disengage in post op period requiring intervention

FDADec 23, 2005AL, CA, CO +4 more• Blackstone Medical Inc.

Abbott Laboratories Diagnostic Div: Clinical Chemistry Multiconstituent Calibrator--- List nu...

The two Multiconstituent Calibrator (MCC) lot numbers 19906M200 and 20879M100 failed to meet product performance expectations throughout the labeled expiration period, as a result of the shortened expiration dating, two lots are now expired. The expiration date for Lot number 26674M100 will be revised from 2006-07-31 to 2006-01-31.

FDADec 23, 2005Nationwide• Abbott Laboratories Diagnostic Div

Polaroid DVD Player Batteries (Petters) – Battery Safety Risk (2005)

The recall involves external battery packs used with the Polaroid-brand portable DVD players in 7-inch and 8-inch screen sizes. The 7-inch DVD player has model number PDV-0700 and the 8-inch player has a model number of PDV-0800. The players and battery packs are silver in color. The battery packs attach to the bottom of the DVD player and have the following serial numbers: DVD Model Number Battery Pack Serial Number Range PDV-0800 060300020000001 through 060300020018000 070300020008001 through 070300020020000 PDV-0700 04170303070001000001 through 04170303070001005000 04270303070001005001 through 04270303070001010000 05040303070001010001 through 05040303070001014000 05150303070001014101 through 05150303070001016100 05190303070001016101 through 05190303070001020100 05260303070001020101 through 05260303070001024100 06010303070001024401 through 06010303070001024900 060300010024101 through 060300010033523 060300010033524 through 060300010050100 070300010050101 through 070300010114100 080300010114101 through 080300010159100 090300010159101 through 090300010193100

CPSCDec 22, 2005Nationwide• Petters Consumer Brands LLC, of Minnetonka, Minn.