FDA Medical Device Recalls (openFDA)
Bemis Health Care,Inc: 5 Qt. Wallmount Sharps Container, Model 150, Regular Size; colors 202 Beige, 030 Red, 040 Yellow, 24 count containers; Made in USA for: Medline Industries; BEMIS label has Manufactured by Bemis Mtg. Co., Sheboygan Falls, WI.
- Recall number
- Z-0170-2007
- Recalling firm
- Bemis Health Care,Inc
- Product
- 5 Qt. Wallmount Sharps Container, Model 150, Regular Size; colors 202 Beige, 030 Red, 040 Yellow, 24 count containers; Made in USA for: Medline Industries; BEMIS label has Manufactured by Bemis Mtg. Co., Sheboygan Falls, WI.
- Status
- Terminated
- Initiated
- 2006-08-23
- Posted
- 2006-11-16
- Terminated
- 2007-01-04
- Reason
- The 5 Quart Wall Safes are shipped as two pieces (bottom & top) that customers are unable to assemble because of excess warp in the back wall of the container.
- Root cause
- Other
- Action
- Letters were mailed to consignees August 23, 2006 describing the product with lots and model numbers. Customers were asked to have product destroyed rather than returned to Bemis. Enclosed with the letter was a Recall Acknowledgement/Destroy in field form that they were instructed to fax to BEMIS. A second letter was sent out to the non-responders on September 13, 2005.
- Quantity
- 145,656 Units
- Distribution
- Nationwide and Canada.
- Lot, serial or model codes
- BEMIS: Model 7H150 020 includes lot 20060001 to 20060016; BEMiS: Model 7H150 030 includes lot 20050006, 20060001 to 20060008; BEMIS: Model 7H150 040 includes lot 20060001 to 20060008; Medline Model 7H950 030 includes lot 20050027, 20060001 to 20060008.
- 510(k) numbers
- ["K931664","K941664"]
- PMA numbers
- not on file
- Product code
- MMK
- Firm FEI
- 2126626
- 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
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
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