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
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Bemis Health Care, Inc
Lot Codes / Batch Numbers
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.
Products Sold
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.
Bemis Health Care, Inc is recalling 5 Qt. Wallmount Sharps Container, Model 150, Regular Size; colors 202 Beige, 030 Red, 040 Yellow, 24 due to 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 c. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
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