🔍 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
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9,636
Consumer Products

Rotating Large Craniotome

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 →

MR GHIATAS Beaded Breast Localization Wire, Product Code: 477201, 479201 Product Usage: The GHIATAS Beaded Breast Localization Wire consists of an introducer needle and asemi-rigid localization wire that are intended for use during breast lesion surgery as a guidefor the surgeon to follow in the excision of the lesion. Product Codes 47020, 475201, 477201,479201, and 470201 do not have the ultrasound enhancement shown in Figure 1. In addition,Product Codes 475201, 477201, 479201, and 470201 may be placed under MRI guidance. .

Bard Peripheral Vascular

🏥 Medical Devices Class I - Dangerous

It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast Localization Wire instead of a MR compatible GHIATAS Beaded Breast Localization Wire.

Mar 28, 2017 Surgical Instruments Nationwide View Details →

5.0cm Short 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 →

8cm 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 →

Dressing M/U XL, P/N 02344 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 →