MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-03-28 for BODY V-T LUMBAR RETR FRAME F/MULTPL B S-0440-1 manufactured by Carefusion, Inc.
[71279922]
(b)(4) on 07mar2017, writer sent the customer an email acknowledging receipt of the complaint, providing the complaint tracking number and requested follow up information including as to if there was any patient impact related to this event. Writer provided contact information. The device is not available for evaluation.
Patient Sequence No: 1, Text Type: N, H10
[71279923]
Medwatch report mw5067803 received states: during procedure, doctor noticed that screw from the versatrac retractor arm was missing, instrument still functioned as need: floor was searched and doctor examined wound to look for screw, but none was discovered; unsure whether screw was in the instrument when the case was started or not. X-ray was taken and radiologist called to room to report not seeing screw on the film either. On10mar2017, additional information: can you please provide your title? Risk analyst if noticed during patient use: was there any patient injury or intervention? No. What was the patient? S medical status after the event? (stable? ) yes. Were there any retained objects? No. Did the patient require an additional medical procedure such as an x-ray? Yes. Was the procedure completed as planned? Yes. Facility information not provided within report. Multiple part numbers reported in medwatch, (b)(4) captures second instrument. No further information available.
Patient Sequence No: 1, Text Type: D, B5
[80323502]
(b)(4): one (1) s-0440-1 body v-t lumbar retr frame f/multpl b was reported as the complaint. The sample was not returned for evaluations, no pictures or further evidence were sent for review and no lot code was reported for the sample. The sample? S condition or age is unknown. The s-0440-1 retractor product has particularly long arms for flexibility of usage. The retractor is intended to function with the s-0435 blade holder and muscle blades: muscle blades are attached separately to the ball snap assembly on the s-0435 part. These blades come in direct contact with the area of surgery on the patient. The customer reported missing screw on the sample during a surgical procedure. It was inferred from the customer description that customer did not know when the screw went missing, the screw could not be found upon searching surrounding areas and operation room. The screw was not found in the patient? S body following an x-ray check by radiologist. Patient injury was not noted. It was not reported exactly which screw on the sample was missing. There are 3 screws installed by manufacturing on the s-0440-1 products: 1 screw (ta-0157) per each arm? S joint/hinge for a total of 2 and 1 (ta-0003) screw that holds the ratcheting lever and spring assembly. It should be noted that the ta-0157 and ta-0003 screws are all pressed/peened in place after screwing in to avoid backing out or loosening. It is not known exactly how the screw loosened and backed out. It is also not known how or if the customer inspected or tested the sample product prior to use. Most probable root causes could be insufficient pre-inspections, intentional disassembly, cleaning related wear, manufacturing error and/or old age. Further analysis and root cause confirmation cannot be completed due to no sample received for review. It should be noted that all screws on the s-0440-1 and similar products are not meant to be removed or disassembled. The screws are pressed/peened in place to avoid backing out and loosening. Conclusion(s): no sample was returned for evaluations and root cause determination. The reported missing component failure mode and possible root causes cannot be verified for final conclusion without sample or photos review. It should be noted that the general ifu for neuro-spine products states that any disassembly of products needed for general maintenance and cleaning should not require a mechanical tool (i. E. Screwdriver). The ta-0157 screw is secured into place and not meant to be disassembled by end user. For any further issues and missing screws, it is recommended to replace or repair the parts of s-0440-1 and other similar products, by sending to the authorized national repair center: (b)(4). (b)(4).
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1923569-2017-00041 |
| MDR Report Key | 6440071 |
| Date Received | 2017-03-28 |
| Date of Report | 2017-06-05 |
| Date of Event | 2016-12-22 |
| Date Mfgr Received | 2017-06-01 |
| Date Added to Maude | 2017-03-28 |
| 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 | 3 |
| Event Location | 3 |
| Manufacturer Contact | ANNA WEHRHEIM |
| Manufacturer Street | 75 NORTH FAIRWAY DRIVE |
| Manufacturer City | VERNON HILLS IL 60061 |
| Manufacturer Country | US |
| Manufacturer Postal | 60061 |
| Manufacturer G1 | CAREFUSION, INC |
| Manufacturer Street | 5 SUNNEN DR |
| Manufacturer City | ST. LOUIS MO 63143 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 63143 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BODY V-T LUMBAR RETR FRAME F/MULTPL B |
| Generic Name | RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY |
| Product Code | GZT |
| Date Received | 2017-03-28 |
| Model Number | S-0440-1 |
| Lot Number | NOT PROVIDED |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAREFUSION, INC |
| Manufacturer Address | 75 NORTH FAIRWAY DRIVE VERNON HILLS IL 60061 US 60061 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-03-28 |