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Becton Dickinson Infusion Therapy

Becton Dickinson Infusion Therapy Recalls

All product recalls associated with Becton Dickinson Infusion Therapy.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 20781–20800 of 21319 recalls

Becton Dickinson Infusion Therapy: BD Introsyte-N Precision Introducer in 1.9Fr. Bulk, Non-s...

Splittable catheter introducer may not fully split or may separate non-uniformly.

FDAFeb 3, 2004Nationwide• Becton Dickinson Infusion Therapy

Becton Dickinson Infusion Therapy: BD First PICC Introsyte-N, 1.9Fr. x 50cm Single Lumen Pr...

Splittable catheter introducer may not fully split or may separate non-uniformly.

FDAFeb 3, 2004Nationwide• Becton Dickinson Infusion Therapy

Richard Wolf Medical Instruments Corp.: Pump Tube, REF 8170,121; Suction Pump Drain Tube; An acce...

If the drain tube is assembled incorrectly, the suction pump will not operate as intended.

FDAFeb 2, 2004

1...1038 103910401041 1042...1066

Page 1040 of 1066Next

NE, TX

• Richard Wolf Medical Instruments Corp.

Becton Dickinson & Company: BD Test Strips. The US market BD Test Strips are ide...

39 lots of BD Test strip may produce an increased frequency of E-3 messages when used during blood glucose testing.

FDAJan 29, 2004Nationwide• Becton Dickinson & Company

Medtronic Xomed, Inc.: The product is a sheath meant to fit over a Nasopharyngos...

The sheaths in question have shafts that are one inch longer than required for the endoscope specified on the label.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Becton Dickinson & Company: The BD Blood Glucose Monitoring Systems identified as the...

39 lots of BD Test strip may produce an increased frequency of E-3 messages when used during blood glucose testing.

FDAJan 29, 2004Nationwide• Becton Dickinson & Company

Medtronic Xomed, Inc.: Product is a surgical nasal/sinus surgical device labeled...

The curve in the shaft of the bur was only 15 degrees not the labeled 40 degrees.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic Xomed, Inc.: Product is a device used in adenoid surgery and is labele...

The box label indicates that the product is a size 2 whereas a size 4 was packed inside.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic MiniMed: Medtronic MiniMed Model 7311 Version 5.0B Solutions Pumps...

A minor software anomaly results in an error in the calculation of the average glucose range that appears on one of the reports available in the model 7311 software.

FDAJan 28, 2004Nationwide• Medtronic MiniMed

Boston Scientific Corporation: Wallstent Rx Biliary Endoprosthesis with Unistep Plus Del...

Incorrect label states stent covered with 'Permalume Covering', product is uncovered

FDAJan 28, 2004CA, GA, MD +4 more• Boston Scientific Corporation

Toshiba American Med Sys Inc: Magnetic Resonance Imaging, System: Flexart, Visart and E...

Software anomally causes image slices to be in incorrect order.

FDAJan 27, 2004CA, CO, FL +10 more• Toshiba American Med Sys Inc

GE Medical Systems Information Technologies: Dinalink brand Communication Cable which is an accessory ...

The potential exists for external electrical noise to be processed as irregular pacing thereby masking potential asystole events.

FDAJan 27, 2004FL, GA, IN +5 more• GE Medical Systems Information Technologies

Stryker Medical: Stryker brand Adel maternity bed, model 4700, with night ...

A potential shock hazard exists if the night light is damaged.

FDAJan 26, 2004Nationwide• Stryker Medical

Smiths Medical ASD, Inc: Portex Tracheal Tube Guide 15 Fr, non-sterile Catalog Nu...

Tracheal tube guide mislabeled as a 15 Fr instead of a 10 Fr

FDAJan 26, 2004CA, CO, FL +10 more• Smiths Medical ASD, Inc

Stryker Medical: Stryker brand Firstcare Ultra Maternity bed, model 5010, ...

A potential shock hazard exists if the night light is damaged.

FDAJan 26, 2004Nationwide• Stryker Medical

Pioneer Surgical Technology: Stayfuse brand intramedullary bone screw; MID 3.8 x 6 mm....

Product labeled as size 3.8x6 mm implant may actually be size 4.3x6 mm implant.

FDAJan 20, 2004Nationwide• Pioneer Surgical Technology

Acrylic Nail Primer (Sassi America) – Chemical Concern (2004)

The primer is packaged in amber-colored bottles with black caps. The model number 508, 509, 510, 511 or 512 is written on the front of the label. "SASSI" also is written on the labels. The primer was sold in .25-ounce, .50-ounce, 1-ounce, 2-ounce and 4-ounce size bottles. The acrylic primers were sold separately and in kits.

CPSCJan 20, 2004Nationwide• Sassi America Inc., of Elk Grove Village, Ill.

DeRoyal Surgical Tray: Multidex Powder, Maltodextrin Wound Dressing, Catalog Num...

Hydrophilic powder wound dressing, sterilized at a dosage which subsequently failed a sterility audit, was distributed.

FDAJan 19, 2004Nationwide• DeRoyal Surgical Tray

Depuy Orthopaedics, Inc.: P.F.C. Modular Knee System Modular Plus Tibial Wedge 10...

Screw size included in system was incorrect

FDAJan 15, 2004IA• Depuy Orthopaedics, Inc.

Wilson-Cook Medical Inc: Four Shooter Saeed Multi-Band Ligator

Product label lacks the symbols specifying the meaning of the manufacturing and expiration date.

FDAJan 15, 2004CA, IN• Wilson-Cook Medical Inc