Propper Mfg Co Inc Propper short gas-chex EO sterilization indicators, 250 strips per box, Reorder No. 269001, Propper Manufacturing Co., Inc., Long Island City, N.Y. 11101 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Propper short gas-chex EO sterilization indicators, 250 strips per box, Reorder No. 269001, Propper Manufacturing Co., Inc., Long Island City, N.Y. 11101
Brand
Propper Mfg Co Inc
Lot Codes / Batch Numbers
Reorder No. 269001, Lots 6081, 6043, 6021, 7042, and 7013
Products Sold
Reorder No. 269001; Lots 6081, 6043, 6021, 7042, and 7013
Propper Mfg Co Inc is recalling Propper short gas-chex EO sterilization indicators, 250 strips per box, Reorder No. 269001, Propper due to The firm discovered a production specification discrepancy that may cause the indicators to show an inaccurate result.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm discovered a production specification discrepancy that may cause the indicators to show an inaccurate result.
Recommended Action
Per FDA guidance
On 2/07/08, Propper Mfg. Co. sent URGENT: DEVICE RECALL letters (dated 2/07/08) to the direct consignees, informing them of the recall of the affected lots of Gas-Chex EO Indicator Strips. The letters also instructed them to: (1) check their inventory to determine if they have the recalled lots in stock; (2) discontinue use of the affected lots; (3) reprocess any unused packs that have been processed with the affected lots of Gas-Chex EO Indicator Strips with non-recalled lots or an alternative product from another supplier; (4) return the affected lots to Propper Manufacturing; (5) complete the enclosed form and return via fax to Propper Mfg. Propper Mfg. will send a postage-paid label and instruction for return of the product, and will ship replacement product as soon as possible. Propper also recommended that consignees review the risk associated with items that have been monitored with the subject chemical indicators although a sterilization cycle failure is unlikely due to equipment controls and other monitoring methods. For questions, please contact Propper at 1-800-832-4300 during regular business hours (9 am to 4:30 pm).
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