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FDA Medical Device Recalls (openFDA)

Exact Medical Manufacturing, Inc.: Probe Cover 6" x 96" regular PE w/ 3 Elastic Bands- Ultrasonic Transducer Cover Item ID: A-AU-0778NA

Recall number
Z-1908-2021
Recalling firm
Exact Medical Manufacturing, Inc.
Product
Probe Cover 6" x 96" regular PE w/ 3 Elastic Bands- Ultrasonic Transducer Cover Item ID: A-AU-0778NA
Status
Terminated
Initiated
2021-04-29
Posted
not on file
Terminated
2022-05-26
Reason
No 510k for the product to be used in a natural or surgical opening to the body
Root cause
No Marketing Application
Action
Exact Medical issued Correction Notification via email on 4/29/21. Letter states: Exact Medical Manufacturing Ultrasonic Transducer Cover can be used to minimize contamination between patient and ultrasound probe during ultrasound scanning procedures for external intact skin. This may help with easier cleaning and disinfection of the probe. This product is not to be used in a natural or surgical opening to the body. The Exact Medical Manufacturing Ultrasonic Transducer Cover are also sold as bulk non-sterile, single use items, to repackers/relabelers establishments for further packaging and ethylene oxide sterilization. These are the boundaries and limitations of use for existing Probe/Transducer cover products in any existing stock from Exact Medical Manufacturing, Inc Further instructions will be given at a future date and we encourage you to reach out with any questions or concerns regarding this issue.
Quantity
1600 units
Distribution
US distribution to states of FL, MT, NY, OH, GA, and Puerto Rico
Lot, serial or model codes
Lot Numbers: 1908E209  1908E435  2005E171  2007E030
510(k) numbers
not on file
PMA numbers
not on file
Product code
ITX
Firm FEI
3008011779
Firm city
Lancaster
Firm state
NY
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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