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
/
Medical Plastics Devices Inc

Medical Plastics Devices Inc Recalls

All product recalls associated with Medical Plastics Devices Inc.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 34301–34320 of 37665 recalls

Medical Plastics Devices Inc: One Touch Basic/Profile Blood Glucose test strips

Counterfeit Glucose Test Strips (manufacturer unknown)

FDAOct 13, 2006Nationwide• Medical Plastics Devices Inc

Boston Scientific Target: Boston Scientific brand Renegade 18 Fiber braided microca...

Incorrect expiration date: The product's exterior box date may be labeled with a longer than actual expiration date (the pouch label is correct)

FDAOct 13, 2006Nationwide• Boston Scientific Target

Medical Plastics Devices Inc: One Touch Ultra Blood Glucose Test Strips

Counterfeit Glucose Test Strips (manufacturer unknown)

FDAOct 13, 2006Nationwide

1...1714 171517161717 1718...1884

Page 1716 of 1884Next

• Medical Plastics Devices Inc

Philips Medical Systems North America Co. Phillips: Allura X-per FD 10/10 x-ray, and fluoroscopy

Potential for generator to lock-up. Fluoroscopy and x-ray is no longer possible, and system must be restarted to be able to continue.

FDAOct 12, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD 20/10 x-ray, and fluoroscopy

Potential for generator to lock-up. Fluoroscopy and x-ray is no longer possible, and system must be restarted to be able to continue.

FDAOct 12, 2006Nationwide• Philips Medical Systems North America Co. Phillips

GE OEC Medical Systems, Inc: OEC InstaTrak 3500, picture archiving and communications ...

GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the potential for the cart to tip over when the arm of the imaging device is extended during use.

FDAOct 11, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC InstaTrak 3500, picture archiving and communications ...

GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the potential for the cart to tip over when the arm of the imaging device is extended during use.

Class IIModerate

FDAOct 11, 2006Nationwide• GE OEC Medical Systems, Inc

Fisher & Paykel Healthcare Ltd 15 Maurice Paykel Place Auckland New Zealand: Fisher & Paykel IW930 CosyCot Infant Radiant Warmer (wit...

This firm has received Product Complaint Reports concerning bending of the pivot plate. The elevator base of the CosyCot Infant Warmer incorporates a pivot plate which forms part of the mechanism allowing the CosyCot to raise and lower in height. A bent pivot plate generally results in the Warmer being unable to elevate properly. Other component failures may result.

FDAOct 9, 2006Nationwide• Fisher & Paykel Healthcare Ltd 15 Maurice Paykel Place Auckland New Zealand

St Jude Medical CRMD: St. Jude Medical Identity SR Model 5172, Identity DR Mode...

St. Jude Medical has identified a low-frequency anomaly in the software used in the APS III Model 3500/3510 and Merlin PCS Model 3650 programmers that can lead to incorrect reporting of battery voltage, expected battery longevity and Elective Replacement Indicator (ERI) status.

FDAOct 6, 2006IN• St Jude Medical CRMD

St Jude Medical CRMD: St. Jude Medical APS III Programmer, used in combination ...

FDAOct 6, 2006IN• St Jude Medical CRMD

Konica Minolta Medical Imaging USA, Inc.: Konica Minolta PrintLink III Model - ID/IV, code no. 07...

The power supply of a unit located in Japan overheated and caused a smoke condition and a small amount of flame coming off the unit.

FDAOct 6, 2006Nationwide• Konica Minolta Medical Imaging USA, Inc.

Boston Scientific: Boston Scientific Medi-Tech Stainless Steel Greenfield Ve...

One lot of product, Stainless Steel Greenfield Vena Cava Filter, may have the incorrect expiration date of 2008-07 and the correct date is 2008-06.

FDAOct 6, 2006Nationwide• Boston Scientific

St Jude Medical CRMD: St. Jude Medical Merlin PCS Programmer, used in combinati...

FDAOct 6, 2006IN• St Jude Medical CRMD

Stryker Howmedica Osteonics Corp.: Duracon Total Knee Distal Femoral Locking Screw for 5 mm ...

Stryker Orthopaedics became aware that a box labeled as Duracon Total Knee Distal Femoral Locking Screws for 5 mm spacer, may actually contain a 10 mm screw.

FDAOct 5, 2006Nationwide• Stryker Howmedica Osteonics Corp.

St. Jude Medical Daig Division: FastCath Transseptal Catheter Introducers with Hemostasis...

Limited number of FastCath Transseptal Catheter Introducers (REF #406850) are susceptible to the irrigation extension tube on the side port becoming disconnected when a pull force is applied.

FDAOct 5, 2006Nationwide• St. Jude Medical Daig Division

Compact Snow Throwers (MTD) – Wheel Burst Risk (2006)

Laceration Risk

The recalled two-stage compact snow thrower is used for snow removal. The snow thrower has two wheels and comes in red, green, gray or black. Troy-Bilt, Yard Machines or Craftsman is printed on the snow thrower's housing. The model number is located on the snow thrower's rear frame. The model numbers included in this recall are listed below. Brand Model Snow Thrower Troy-Bilt 31AS3BB2766 5.5 HP 24-inch Two-Stage Yard Machines 31A-3AAD700 5 HP 22-inch Two-Stage 31A-3BAD700 5.5 HP 22-inch Two-Stage 31A-3BAD729 5.5 HP 22-inch Two-Stage 31A-3BAD752 5.5 HP 22-inch Two-Stage 31A-3BAD762 5.5 HP 22-inch Two-Stage 31AS3DDE729 7 HP 24-inch Two-Stage Craftsman 247.88255 5.5 HP 24-inch Two-Stage 247.88700 5 HP 22-inch Two-Stage

CPSCOct 5, 2006Nationwide• MTD Products Inc, of Cleveland, Ohio

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

Laborie Medical Technologies: Laborie Transducer Cartridge with Luer Lock Reference: DI...

Mislabeling: Product labeled with incorrect "Use Before" date and pouch labels missing lot number. (Incorrect dates-2006/07 or 2006/08; correct Use by dates-2009/08 for Lot 36H03M005 and 2009/07 for Lot 36G20M041

FDAOct 4, 2006AR, CA, FL +5 more• Laborie Medical Technologies

Southern Prosthetic Supply Co.: SPS Blue Line Tube Clamp Adapters, Product No. BL120M

Device Fracturing: recent design and process changes leave the device susceptible to fracturing, which could cause the prosthesis to fail

FDAOct 3, 2006Nationwide• Southern Prosthetic Supply Co.