Device recalls

SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.

Ethicon, Inc. · Some applicator tips from these lots had open seals.

Open, ClassifiedUnder Investigation by firmZ-1881-2024
Open FDA's page for this record
Cfres ID
207318
Product res number
Z-1881-2024
Event date initiated
2024-04-23
Event date posted
2024-05-22
Recall status
Open, Classified
Res event number
94496
Product code
LMF
Product description
SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.
Code info
Product Number: 1979, UDI/DI: 15712123000264, Lot/Serial Numbers: 272574, 272369 and 272770.
Firm FEI number
2210968
Recalling firm
Ethicon, Inc.
Address 1
Us Highway 22 West
City
Somerville
State
NJ
Postal code
08876
Additional info contact
Ethicon Resource Department 908-218-0707
Reason for recall
Some applicator tips from these lots had open seals.
Root cause description
Under Investigation by firm
Product quantity
5,184 units
Distribution pattern
US Nationwide distribution in the states of AR, CA, FL, GA, ID, IL, IN, KY, MA, MD, MN, MO, NC, NE, NJ, PA, TN, TX, WI.
Action

On April 19, 2024 Urgent Medical Device Recall (Removal) letters were distributed to distributors and customers. Actions to be taken by customer: 1. Examine your inventory immediately to determine if you have product subject to this recall on hand and quarantine such product(s). If you have product subject to this recall, please maintain a copy of this notice with the quarantined product and keep a copy for your records. 2. Communicate the issue to relevant operating room or materials management personnel, or anyone else in your facility who needs to be informed. If any product subject to this recall has been forwarded to another facility, contact that facility to arrange return. Please consider including a copy of this recall letter when communicating. 3. Complete the Business Reply Form (BRF) (Attachment 2) confirming receipt of this notice and fax or email to Sedgwick at 844-656-8030 or ethicon4908@sedgwick.com within three (3) business days. Please return the BRF even if you do not have product subject to this recall. 4. Customers are required to return unused SURGIFOAM" Absorbable Gelatin Powder Kits subject to this recall that are in inventory immediately. To receive credit, customers must return product subject to this recall no later than July 31, 2024. The entire kit must be returned. Any non-affected product and any product returned after the date specified will not receive credit. 5. To return product subject to this recall, photocopy the completed BRF, place it in the box with the product, and affix the pre-paid authorized shipping label included with the recall notification letter. Ethicon will pay for the shipping charges only if the authorized label is used. Extra shipping labels may be obtained by calling Sedgwick at 866-912-8413. Your account number and mailing address have been pre-populated on the BRF. 6. Keep this notice visibly posted for awareness until all product subject to this recall has been returned to Sedgwick. If you require any assista

PMA numbers
P990004
Harmonized identifiers (openFDA)
Device name
Agent, Absorbable Hemostatic, Collagen Based
Medical specialty description
General, Plastic Surgery
Regulation number
878.4490
Device class
3
PMA number
P850010, P830079, P930030, P810006, P850023, P990004, N18286, P810040, P050044, P990030, P800002, N17600, P990009
Registration number
1810189, 3035387162, 2648988, 1319639, 3011689956, 3009337401, 2650143, 2029275, 1213643, 3003120666, 3010132111, 1225991, 2937398, 3002907620, 3006405073, 3011137372, 1121308, 3007766601, 3014579161, 3016844398, 2134812, 3014272734, 1000150646, 3003418325, 3002807315, 2953359, 3007162296, 2528981, 3008478369, 1223089, 2024024, 2011171, 3012187973, 3012421607, 1416980, 3004425647, 3014461810
FEI number
1810189, 3035387162, 1416980, 3011689956, 3009337401, 3000204775, 3002827704, 1213643, 3003120666, 3010132111, 1000138054, 1000306431, 3002516348, 2937398, 3002907620, 3006405073, 1121308, 3007766601, 3014579161, 3016844398, 3014272734, 1000120505, 3003418325, 3002807315, 3000215205, 3007162296, 2528981, 3005747797, 3008478369, 2648209, 2024024, 2011171, 3012187973, 3012421607, 3004393730, 3004425647, 3014461810
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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.