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FDA Medical Device Recalls (openFDA)

Bemis Manufacturing Co.: Bemis Two-Gallon Sharps Container, Models #102 020, #102 030, and #102 040. (The only difference between the models is in color. Model 102 040 is yellow, Model 102 020 is beige and Model 102 030 is red. )

Recall number
Z-0789-04
Recalling firm
Bemis Manufacturing Co.
Product
Bemis Two-Gallon Sharps Container, Models #102 020, #102 030, and #102 040. (The only difference between the models is in color. Model 102 040 is yellow, Model 102 020 is beige and Model 102 030 is red. )
Status
Terminated
Initiated
2004-02-25
Posted
2004-07-20
Terminated
2004-06-24
Reason
The closure flap of the recalled sharps containers have two tabs that fit into slots on the cover for final closure and locking but some of the covers have one of the tabs that will not fit into the designated slot because the slot is occluded with plastic.
Root cause
Other
Action
Recall letters dated 2/25/04 requested the return of the product and providing for notification of the subaccounts that may have received the product.
Quantity
1920 containers
Distribution
The recalled containers were shipped to consignees in Connecticut, Florida, Georgia, Pennsylvania and Tennessee in the United States, and to a consignee in Canada.
Lot, serial or model codes
Lot #20040001 and Lot #20040004
510(k) numbers
["K965248"]
PMA numbers
not on file
Product code
MMK
Firm FEI
3000209940
Firm city
Sheboygan Falls
Firm state
WI
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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