MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2011-08-17 for UNI-SOLVE WIPES 402300 manufactured by Smith & Nephew Wound Management.
[2203567]
This unsolved complaint that was received post smith & nephew's remedial action (voluntary recall) to prevent an unreasonable risk of substantial harm to the public health (ref. Recall #3006760724-04-06-2011-001r). Patient has been in and out of (b)(6) located in (b)(4) since (b)(6) 2011. Patient diagnosed with having diarrhea. Patient will be going to (b)(6) for testing to find out what's causing the reoccurrences of diarrhea. Patient sister wondering if her sister's diarrhea is associated with smith & nephew recall wipes. Patient developed pneumonia while in (b)(6).
Patient Sequence No: 1, Text Type: D, B5
[9218956]
Active investigation in progress; investigation results will be provided in a supplement report. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[9556820]
No product was returned by the customer. Other return samples of the reported lots 0k209 and 0h229 were analyzed by an independent test laboratory and met finished product specifications with no evidence of microbial contamination found. Batch records for the lots indicate all specifications were met at the time of release and no inconsistencies were noted. An independent medical review concluded there was no correlation between the reported symptoms and the use of uni-solve wipes.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 3006760724-2011-00016 |
| MDR Report Key | 2214876 |
| Report Source | 04 |
| Date Received | 2011-08-17 |
| Date of Report | 2011-08-16 |
| Date of Event | 2011-07-25 |
| Date Mfgr Received | 2011-07-25 |
| Date Added to Maude | 2011-08-22 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | MR TERRY MCMAHON |
| Manufacturer Street | 970 LAKE CARILLON DRIVE SUITE 110 |
| Manufacturer City | ST. PETERSBURG FL 33716 |
| Manufacturer Country | US |
| Manufacturer Postal | 33716 |
| Manufacturer Phone | 7273993785 |
| Manufacturer G1 | SMITH & NEPHEW WOUND MANAGEMENT |
| Manufacturer Street | 970 LAKE CARILLON DRIVE SUITE 110 |
| Manufacturer City | ST. PETERSBURG FL 33716 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 33716 |
| Single Use | 0 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | UNI-SOLVE WIPES |
| Generic Name | SOLVENT, ADHESIVE TAPE |
| Product Code | KOX |
| Date Received | 2011-08-17 |
| Model Number | 402300 |
| Catalog Number | 402300 |
| Lot Number | 0H229 |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SMITH & NEPHEW WOUND MANAGEMENT |
| Manufacturer Address | 970 LAKE CARILLON DRIVE SUITE 110 ST. PETERSBURG FL 33716 US 33716 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 2011-08-17 |