Device recalls

Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray

MEDLINE INDUSTRIES, LP - Northfield · Trumpet Needle Guide ring can detach when excessive pressure is applied.

Open, ClassifiedProcess controlZ-1917-2024
Open FDA's page for this record
Cfres ID
207231
Product res number
Z-1917-2024
Event date initiated
2024-03-01
Event date posted
2024-05-29
Recall status
Open, Classified
Res event number
94448
Product code
LRP
Product description
Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray
Code info
UDI/DI 40653160122945 (case), 10653160122944 (unit), Lot Numbers: 23JBX257, 23KMG455
Firm FEI number
1417592
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Address 1
3 Lakes Dr
City
Northfield
State
IL
Postal code
60093-2753
Additional info contact
Karin Johnson 886-359-1704
Reason for recall
Trumpet Needle Guide ring can detach when excessive pressure is applied.
Root cause description
Process control
Product quantity
30 units
Distribution pattern
US Nationwide distribution.
Action

Medline issued a correction notice to its consignees on 03/01/2024 via email and USPS first class mail. The notice explained the issue and requested the consignee identify and quarantine all affected products, and respond to the notice. Once the response was received Medline would provide labels to place over the affected product in stock. If the product was further distributed the party which distributed the product was directed to notify their customers.

Harmonized identifiers (openFDA)
Device name
Tray, Surgical
Medical specialty description
General, Plastic Surgery
Regulation number
878.4800
Device class
1
K number
K883098, K890071, K940444, K903963, K951811, K935621, K940239, K874665, K963723, K873439, K905462, K881095, K873290, K912105, K922126, K873469, K940646, K760497, K861142, K882275, K903962, K903544
Registration number
1043534, 3006636962, 3006554788, 1835444, 1030451, 3004111573, 3009756153, 3009140376, 3016171961, 3008534770, 3038613790, 3017410889, 3003759558, 1721686, 3005075853, 3002821232, 3012944064, 3005182241, 3015876273, 3013503739, 3005245797, 3003431869, 3005071827, 1422507, 3027320022, 1421879, 3007494564, 3008747271, 1056350, 1834379, 1030489, 3025663209, 3002675176, 3003032798, 3027305775, 3004122598, 3006272282, 3010829427, 1648571, 1928237 +247 more
FEI number
1043534, 3006636962, 3006554788, 3002807830, 1030451, 3004111573, 3009756153, 3009140376, 3016171961, 3007329020, 3008534770, 3005985723, 3038613790, 3003759558, 1721686, 3005075853, 3002821232, 1000115331, 3012944064, 3005182241, 3015876273, 3013503739, 3005245797, 3003431869, 3005071827, 3004150667, 3027320022, 3002807264, 1000514656, 1000402972, 3007494564, 1000140363, 3008747271, 3003040625, 3025663209, 3002675176, 3003032798, 3027305775, 3004122598, 3006272282 +246 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.