🔍 RecallPedia

All Recalls

95,083 total recalls in our database

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28,983
Food
 💊
17,685
Drugs
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38,779
Medical Devices
 🏠
9,636
Consumer Products

Reciprocating MICRO SAW

The Anspach Effort

🏥 Medical Devices Class I - Dangerous

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Oct 6, 2016 Other Medical Devices Nationwide View Details →

Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between 2003 and 2008. Catalog Part Number 010066. Top Assembly Part Numbers: 040906, 040904, 040756, 040758, 040658, 040680. Product Usage: Device is used to provide treatment for neonatal hyperbilirubinemia.

Natus Medical Incorporated

🏥 Medical Devices Class I - Dangerous

The second generation neoBLUE 2 lights with a black band, sold from 2003 to 2008, are recalled so it will eliminate the possibility that a neoBLUE system may have a replacement board installed which allows it to be used at a higher overall light intensity than the devices were originally cleared to deliver.

Apr 3, 2017 Other Medical Devices Nationwide View Details →

Dressing, Knee L/XL, P/N 04708 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be applied in a sterile environment. Breg has determined that a small percentage (approximately 0.22%) of these products may have been sent with unsealed pouches by the contract manufacturer. Customers will be contacted and instructed to inspect their inventory for any product with unsealed pouches and discard them.

Breg

🏥 Medical Devices Class I - Dangerous

They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.

Mar 30, 2017 Implants & Prosthetics Nationwide View Details →

7.5cm QD Angle Attachment

The Anspach Effort

🏥 Medical Devices Class I - Dangerous

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Oct 6, 2016 Other Medical Devices Nationwide View Details →

Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.

Terumo Medical

🏥 Medical Devices Class I - Dangerous

Based on internal investigation and testing that revealed the distal end of certain lots of Terumo Medical Destination¿ products may not contain the labeled 5 cm of coating. While there have been no complaints or patient related incidents reported, the lack of coating could render it difficult to navigate the device to the target vasculature.

Nov 6, 2015 Diagnostic Equipment Nationwide View Details →

Dressing Back, P/N 09810 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be applied in a sterile environment. Breg has determined that a small percentage (approximately 0.22%) of these products may have been sent with unsealed pouches by the contract manufacturer. Customers will be contacted and instructed to inspect their inventory for any product with unsealed pouches and discard them.

Breg

🏥 Medical Devices Class I - Dangerous

They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.

Mar 30, 2017 Other Medical Devices Nationwide View Details →

SurFlo IV Catheter

Terumo Medical

🏥 Medical Devices Class I - Dangerous

According to the Terumo (TMC) this device is used to access the human peripheral vascular system for short term use (less than 30 days) for the purpose of infusing fluids into patients. A small percentage of the catheters in the affected lots may have damage to the ETFE catheter which may allow the catheter to break during withdrawal.

Aug 5, 2015 Surgical Instruments View Details →