ConvaTec, Inc Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660, t) 423661 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660, t) 423661
Brand
ConvaTec, Inc
Lot Codes / Batch Numbers
a) 423643, UDI/DI 768455203925, Lot Numbers 3L03391, b) 423658, UDI/DI 768455204076, Lot Numbers 3L04005, c) 423659, UDI/DI 768455204083, Lot Numbers 3L03670, d) 423664, UDI/DI 768455204137, Lot Numbers 3L02230, e) 423666, UDI/DI 768455204151, Lot Numbers 3L04004, f) 423645, UDI/DI 976845520394, Lot Numbers 3L04989, g) 423667, UDI/DI 768455204168, Lot Numbers 3L04674, h) 423657, UDI/DI 768455204069, Lot Numbers 3L04114, i) 423652, UDI/DI 768455204014, Lot Numbers 3L03669, j) 423646, UDI/DI 768455203956, Lot Numbers 3M01542, k) 423654, UDI/DI 768455204038, Lot Numbers 3M00021, l) 423653, UDI/DI 768455204021, Lot Numbers 3M00786, m) 423647, UDI/DI 768455203963, Lot Numbers 3M01540, n) 423644, UDI/DI 768455203932, Lot Numbers 3M01539, o) 423648, UDI/DI 768455203970, Lot Numbers 3M01541, p) 423665, UDI/DI 768455204144, Lot Numbers 3M00029, q) 423656, UDI/DI 768455204052, Lot Numbers 3L00958, r) 423651, UDI/DI 768455204007, Lot Numbers 3K03888, s) 423660, UDI/DI 768455204090, Lot Numbers 3M00022, t) 423661, UDI/DI 768455204106, Lot Numbers 3M00023
Products Sold
a) 423643, UDI/DI 768455203925, Lot Numbers 3L03391; b) 423658, UDI/DI 768455204076, Lot Numbers 3L04005; c) 423659, UDI/DI 768455204083, Lot Numbers 3L03670; d) 423664, UDI/DI 768455204137, Lot Numbers 3L02230; e) 423666, UDI/DI 768455204151, Lot Numbers 3L04004; f) 423645, UDI/DI 976845520394, Lot Numbers 3L04989; g) 423667, UDI/DI 768455204168, Lot Numbers 3L04674; h) 423657, UDI/DI 768455204069, Lot Numbers 3L04114; i) 423652, UDI/DI 768455204014, Lot Numbers 3L03669; j) 423646, UDI/DI 768455203956, Lot Numbers 3M01542; k) 423654, UDI/DI 768455204038, Lot Numbers 3M00021; l) 423653, UDI/DI 768455204021, Lot Numbers 3M00786; m) 423647, UDI/DI 768455203963, Lot Numbers 3M01540; n) 423644, UDI/DI 768455203932, Lot Numbers 3M01539; o) 423648, UDI/DI 768455203970, Lot Numbers 3M01541; p) 423665, UDI/DI 768455204144, Lot Numbers 3M00029; q) 423656, UDI/DI 768455204052, Lot Numbers 3L00958; r) 423651, UDI/DI 768455204007, Lot Numbers 3K03888; s) 423660, UDI/DI 768455204090, Lot Numbers 3M00022; t) 423661, UDI/DI 768455204106, Lot Numbers 3M00023
ConvaTec, Inc is recalling Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423 due to Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for specific lots of the EsteemBody Soft Convex, Drainable Pouch due to inconsi. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for specific lots of the EsteemBody Soft Convex, Drainable Pouch due to inconsistency in the strength of the filter weld.
Recommended Action
Per FDA guidance
ConvaTec issued an URGENT: VOLUNTARY MEDICAL DEVICE RECALL notice to its consignees on 02/19/2024 via email. The notice explained the problem and requested the consignee quarantine the affected product and respond. Upon receipt, the firm will issue a Certificate of destruction and request the destruction of the product. The notice be shared with the correct individual with the organization and disseminated to all who need to be aware and distributors were directed to notify their customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026