Z-1915-2021 Class II Terminated
FDA device recall Z-1915-2021 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: 100600 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
- 100600 units
Product description
Transducer Cover 15x147cm, Kit, VIP Film w/ Bands & EMM Gel Item ID: E6359
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: 2003E690 2006E079 2004E015 2007E001 2006E079 2007E002 2010E361 2101E329 2011E271
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1915-2021
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026