Z-1908-2021 Class II Terminated

Recalled by Exact Medical Manufacturing, Inc. — Lancaster, NY

FDA device recall Z-1908-2021 was initiated by Exact Medical Manufacturing, Inc. on Apr 29, 2021 and is designated Class II. Reason for recall: No 510k for the product to be used in a natural or surgical opening to the body The recall status is terminated (terminated May 26, 2022). Affected quantity: 1600 units.

Recall details

Product Type
Devices
Report Date
Jun 30, 2021
Initiation Date
Apr 29, 2021
Termination Date
May 26, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1600 units

Product description

Probe Cover 6" x 96" regular PE w/ 3 Elastic Bands- Ultrasonic Transducer Cover Item ID: A-AU-0778NA

Reason for recall

No 510k for the product to be used in a natural or surgical opening to the body

Distribution pattern

US distribution to states of FL, MT, NY, OH, GA, and Puerto Rico

Code information

Lot Numbers: 1908E209 1908E435 2005E171 2007E030

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1908-2021
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for Z-1908-2021. Report a data issue: hello@regdatalab.com.