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Pro-Dex Inc dba Dyna-Dent

Pro-Dex Inc dba Dyna-Dent Recalls

All product recalls associated with Pro-Dex Inc dba Dyna-Dent.

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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 6421–6440 of 7756 recalls

Pro-Dex Inc dba Dyna-Dent: Zimmer PTW4321 20 Ncm Dental Torque Wrench, QTY 1 Pro-Dex...

Pro-Dex has initiated a recall on their Dental Torque Wrench. The recall was initiated due to an inaccurate laser etch identification of the torque value.

FDAJan 19, 2009Nationwide• Pro-Dex Inc dba Dyna-Dent

Abbott Laboratories: AxSYM CMV IgG Reagent Pack; Abbott Laboratories, Abbott P...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

Abbott Laboratories: AxSYM CORE 2.0 Reagent Pack; Abbott Laboratories, Abbott ...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR

1...320 321322323 324...388

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• Abbott Laboratories

Abbott Laboratories: AxSYM Myoglobin Reagent Pack, Abbott Laboratories, Abbott...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

Bosch and Siemens Dishwashers (BSH) – Fire Risk (2009)

Fire/Burn Risk

This recall involves certain Bosch® and Siemens® dishwashers manufactured from May 1999 through July 2005. The brand name is printed on the dishwasher's front control panel. Model and serials numbers are located inside the dishwasher door panel on the upper right side. Brand Model Numbers Must Begin With Serial Numbers within the range of Bosch SHE43C, SHE44C SHE46C, SHE56C SHU33 SHU42 SHU432 SHU43C, SHU53A FD8503 - FD8507 FD8501 - FD8505 FD7905 - FD8505 FD8407 - FD8505 FD8004 - FD8211 FD8205 - FD8507 Siemens SL34A FD8308 - FD8505

CPSCJan 15, 2009Nationwide• BSH Home Appliances Corp., of Huntington Beach, Calif.

Biomet Microfixation, Inc.: BD Recalled component is labeled: BD 60ml Syringe Luer-...

Biomet Microfixation, Inc. is recalling their OnPoint TMJ Kit (Part Numbers 24-3050, 24-3055) and Arthrosimplicity TMJ Arthocentesis Kit (Part Numbers 922070, 922090, 922075). These two kits contain a BD sterile disposable 60 ml Luer-Lok syringe, Part number 309653 which is under recall by Becton Dickinson (Recall Number Z-2347-2008). Becton Dickinson has determined that unit package seal integ

FDAJan 9, 2009AL, CA, CT +22 more• Biomet Microfixation, Inc.

Hsmg, Inc. D/b/a Smartinfuser Usa: SmartBlock Pain Management System, Part numbers P49524, P...

Product leaks associated with a new pump reservoir, and incident related to regulator fast priming feature.

FDAJan 8, 2009Nationwide• Hsmg, Inc. D/b/a Smartinfuser Usa

Toshiba American Medical Systems Inc: Aquilion 32 CT System; Model number TSX-101 A/E The pro...

Toshiba America Medical Systems Inc (TAMS) has initiated a field correction on the Aquilion 32 CT Scanners due to the potential for the bolus tracking software (SureStart) to cause delay of the helical scan, up to 10 seconds, when large volumes of data are being reconstructed on the secondary console.

FDAJan 8, 2009Nationwide• Toshiba American Medical Systems Inc

Hsmg, Inc. D/b/a Smartinfuser Usa: SmartInfuser PainPump, part numbers P49230, P49220, P4922...

Product leaks associated with a new pump reservoir, and incident related to regulator fast priming feature.

FDAJan 8, 2009Nationwide• Hsmg, Inc. D/b/a Smartinfuser Usa

Toshiba American Medical Systems Inc: Aquilion 64 CT System; Model number TSX-101 A/D The pro...

FDAJan 8, 2009Nationwide• Toshiba American Medical Systems Inc

BD Biosciences, Systems & Reagents: BD FACS Sample Prep Assistant (SPA and SPA II) Instrument...

To prevent a needle stick while replacing the probe, the firm has initiated a Field Correction, and issued an improved Users Guide procedure (User Bulletin, Part Number 645050).

FDAJan 3, 2009Nationwide• BD Biosciences, Systems & Reagents

Boston Scientific Corporation: Gold Probe 10FR Working Length: 300 cm, Probe Tip O.D. 3....

Packaging tray for the Gold Probe Single-Use BiPolar Electrohemostasis Catheters may have a crack. Cracks in the tray or damage to the tray of the Gold Probe device may lead to a compromised sterile barrier.

FDADec 24, 2008Nationwide• Boston Scientific Corporation

Boston Scientific Corporation: Gold Probe 7FR Working Length: 300 cm, Probe Tip O.D. 2.3...

FDADec 24, 2008Nationwide• Boston Scientific Corporation

Alpine Ski Bindings (Atomic) – Unexpected Release (2008)

The recall affects the heel components of the following Atomic alpine ski bindings: Race 310, Race 412, RaceRace 310, RaceRace 412, Xentrix 310, Xentrix 311, Xentrix 412, C310, C311, C412, CR 310, CR 412, R 310, R 412, SX 310, SX 412, Device 311, Device 412, Centro 310, Centro 412, and Dynamic ADX 312, RD10, X412, Centro 412. The recall includes only those bindings manufactured from 1998 through 2002 The year of manufacture can be located on the underside of the heel lever.

CPSCDec 23, 2008Nationwide• Atomic Skis GmbH, of Austria

Cardinal Health 303 dba Cardinal Health: ReadyMed Elastomeric Ambulatory Pump, Model Numbers: R050...

The recall was initiated as a result of a potential for out of specification flow rates. The product may not consistently meet the labeled flow rate range of +/- 15%.

FDADec 19, 2008Nationwide• Cardinal Health 303 dba Cardinal Health

Migada Inc. P.O Box 888 Kiryat Shmona Israel: TEVADAPTOR Closed Drug Reconstitution and Transfer System...

Syringe adaptor is disintegrating when attached to the end of the syringe.

FDADec 18, 2008Nationwide• Migada Inc. P.O Box 888 Kiryat Shmona Israel

Abbott Laboratories: Hematology Reagent Syringe, List number 08H49-02, used on...

Some syringes were improperly assembled and are therefore not usable, due to an incorrect nut on the syringe shell.

FDADec 10, 2008Nationwide• Abbott Laboratories

Bio-Rad Laboratories Inc: Bio-Rad Variant II Hemoglobin Testing System with CDM v 4...

The wrong barcode number and tube position number may be assigned to samples leading to discrepant sample results.

FDADec 9, 2008Nationwide• Bio-Rad Laboratories Inc

Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.: V-Probe, Endocare Cryo V Probe model # Cryo 206V. The pr...

Endocare received a report of a patient death that occurred during a prostate cryoablation procedure. An autopsy attributed the cause of death to an air embolism. The safety notice for the cryoprobes was issued to refocus attention on the Indications and Safety Review included with the Physician Training Materials and to reinforce additional safety information.

FDADec 5, 2008Nationwide• Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.

C.R. Bard Access Systems, Inc: Bard Access Systems, Inc., Ponsky* PEG (Percutaneous Endo...

Snare can detach in patient. The Polypectomy Snares and the Entake Peg System (which contain these snares) are being recalled because the looped portion of the snare can become detached and drop into the stomach or other internal canal during use, necessitating retrieval of the remaining piece.

FDADec 4, 2008Nationwide• C.R. Bard Access Systems, Inc