Recall Z-1866-2011
Hartmann USA, Inc · initiated February 11, 2011
Product
HydroHydrofilm is for use as a post-operative and primary dressing to protect against secondary infection and to cover non-exudating wounds and for use as a secondary dressing for fixation of catheters or cannulae.film, 10cm x 12.5 cm, Paul Hartmann AG, 89522 Heidenhiem, Germany
Codes / lots: Lot number: 000543118
Reason for recall
Misbranded; the expiry date on the primary packing incorrectly indicates 2010-10, instead of 2015-10. Consignees were notified by letter on/about 02/11/2011. They were advised to examine their inventory and not to use any of the affected product and to return it to Paul Hartmann. A response form was included to be completed and returned to Paul Hartmann. They were further instructed to pass the no
FDA-determined cause: Other
Action taken
Hartmann USA, Inc. sent letter to the Consignees on 2/11/11. They were advised to examine their inventory and not to use any of the affected product and to return it to Hartmann USA, Inc. A response form was included to be completed and returned to Hartmann USA, Inc. They were further instructed to pass the notice on to their consignees if distributed. For questions, call (803) 325-7600.
Details
- Recall number
- Z-1866-2011
- Initiated
- February 11, 2011
- Posted by FDA
- April 1, 2011
- Terminated
- August 12, 2011
- Product code
- MGP – Dressing, Wound And Burn, Occlusive
- Quantity
- 100 boxes (10 x 12.5 cm per box)
- Distribution
- Nationwide -- Including CA, GA, IL, MO, MS, TX, and VA.
- Recalling firm
- Hartmann USA, Inc, Rock Hill, SC