Abbott Medical Radiofrequency Grounding Pad, REF RF-DGP-L Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Radiofrequency Grounding Pad, REF RF-DGP-L
Brand
Abbott Medical
Lot Codes / Batch Numbers
UDI: 05415067028914 Batch Numbers: 810319004, 810319005, and 810319021
Products Sold
UDI: 05415067028914 Batch Numbers: 810319004, 810319005, and 810319021
Abbott Medical is recalling Radiofrequency Grounding Pad, REF RF-DGP-L due to Affected lots were manufactured with the protective release liner in an incorrect orientation. When attempting to remove this disposable release line. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Affected lots were manufactured with the protective release liner in an incorrect orientation. When attempting to remove this disposable release liner, a clear film may be left on the grounding pad which may interfere with patient skin contact and lead to uneven heating.
Recommended Action
Per FDA guidance
The firm initiated the recall by letter hand delivered by an Abbott field representative. The letter requested that consignee cease use of the affected lot and return the product with the aid of a field representative.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026