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Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada

Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada Recalls

All product recalls associated with Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada.

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

Most Recent

Dec 2025

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 4741–4760 of 10937 recalls

SLIM Handle (Pega Medical) – internal connector issue (2019)

Handle could jam with the Driver due to the detachment of an internal Connector Ring.

Moderate

FDAMay 29, 2019CA, DE, FL +5 more• Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada

Quantum Pump Console (Spectrum Medical) – shutdown risk (2019)

Potential for Quantum Pump Console, part of the Quantum Perfusion Systems, to unexpectedly shut down while in use.

Moderate

FDAMay 29, 2019NY, OH, VA +1 more• Spectrum Medical Ltd. Harrier 4, Meteor Business Park Cheltenham Road East Gloucester United Kingdom

Lightning USB Charging Cables (Target) – shock and fire hazard (2019)

Fire/Burn Risk

This recall includes the heyday 3 Foot Lightning USB charging cables. The cables are used to charge cellphones and other electronics that use lightning connector charging cables. The metal charging cable is purple, green and blue iridescent. The word "heyday" is printed on the cable's connector. The model number 080 08 8261 is printed on the side of the product's packaging.

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High

CPSCMay 29, 2019Nationwide• Chug Inc., of Eden Prairie, Minn.

ICS CHARTR EP 200 (GN Otometrics) – electrical shock risk (2019)

There is a risk to the healthcare professional or patient of exposure to undergrounded electrical surfaces which may result in an electrical shock.

High

FDAMay 28, 2019AL, AK, AZ +45 more• GN Otometrics Horskatten 9 Taastrup Denmark

E-Line Cutting Electrode (Richard Wolf) – Incorrect Electrode Package (2019)

Laceration Risk

E-Line Cutting Electrode package 8416.0305 contains E-Line Hook Electrode 8416.09 instead of E-Line Cutting Electrode 8416.03.

Moderate

FDAMay 23, 2019Nationwide• Richard Wolf Medical Instruments Corp.

Havoc ROV (Arctic Cat) – Crash Hazard (2019)

This recall involves all model year 2018 and 2019 Textron Havoc recreational off-highway vehicles manufactured by Arctic Cat. The two-seat vehicles come in four color combinations: charcoal metallic/bronze, green/black, red/black or white/black. The vehicles have Textron Off Road printed on each side of the hood and Havoc on each side of the rear cargo box.

High

CPSCMay 22, 2019Nationwide• Arctic Cat Inc., of Thief River Falls, Minn., a subsidiary of Textron Specialized Vehicles, of Augusta, Ga.

InterStim System (Medtronic) – Stimulation Programming Risk (2019)

There is a potential for an unexpected increase in stimulation during InterStim programming with the A10 Clinician Application (on Medtronic's smart programmer).

High

FDAMay 15, 2019Nationwide• Medtronic Neuromodulation

BD Microtainer LH Tubes (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

BD Microtainer SST (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

BD Microtainer SST Amber (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

BD Microtainer Z Tubes (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

BD Microtainer FE Tubes (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

BD Microtainer K2E Tubes (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

Amitiza Capsules (Mallinckrodt) – Label Mix-up (2019)

Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24 mcg capsules were found in a 8 mcg trade 60 ct. bottle. Amitiza 24 mcg capsules are being recalled because a sealed 60 ct. bottle contained only 8 mcg capsules, this incident is being considered as a labeling mix-up issue.

Class IIModerate

FDAMay 13, 2019Nationwide• MALLINCKRODT PHARMACEUTICALS

Amitiza Capsules (Mallinckrodt) – Labeling Mix-up (2019)

Class IIModerate

FDAMay 13, 2019Nationwide• MALLINCKRODT PHARMACEUTICALS

BD Microtainer PST LH Amber Tube (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

BD Microtainer PST LH Tube (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

Transesophageal Cardiac System (CardioCommand) – Battery Contact Corrosion (2019)

Possible corrosion of the battery contact(s).

Moderate

FDAMay 10, 2019Nationwide• Cardiocommand Inc.

Beckley Entertainment Hutch – injury hazard (2019)

This recall involves the Beckley Entertainment Hutch sold by Havertys in a weathered charcoal finish or a dovetail gray finish. The hutch can house an 80 inch TV in the center. There is an open shelf above and drawers underneath the center space. The hutch is about 69 inches wide, 56 inches tall, and has a label with the SKU on the back. The SKU for the Weathered Charcoal Finish is 0-4000-3197 and the Dovetail Grey Finish is 0-4000-3538.

Moderate

CPSCMay 9, 2019Nationwide• Minh Thanh Company Limited, of Vietnam

Alaris Pump Infusion Set (Becton Dickinson) – Occlusion Potential (2019)

An incomplete occlusion can be caused by a variation in the wall thickness of the pumping segment of the affected infusion sets used with the. The issue has the potential to lead to unintended delivery of medication when the pump module is not in running status or can result in faster than expected drug delivery flow when the pump is infusing.

High

FDAMay 6, 2019Nationwide• Becton Dickinson & Company