Whatman, Inc. Whatman Body Fluid Collection Paper 903 The device is used by healthcare professionals in the collection and in-vitro storage of neonate blood. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Whatman Body Fluid Collection Paper 903 The device is used by healthcare professionals in the collection and in-vitro storage of neonate blood.
Brand
Whatman, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Ref:/Lot number: 10534513 WO71 6794508 10534614 WO71 6795508 10534749 WO71 6795908 10534683 WO71 6800708 10534711 WO71 6807908 10534528 WO71 6800108 10534545 WO71 68235.008 10534578 WO71 6825608 10534782 WO71 6798908 10534640 WO71 6803208 10534639 WO71 6820908 10539765 WO71 6821008 10534523 WO71 6800208 10534524 WO71 6800308 10534691 WO71 6824408 10534523 WO71 6824508 10534611 WO71 6824108 10534647 WO71 6803708 10534648 WO71 6803808 10534735 WO71 6796508 10535643 WO71 6806908 10534670 WO71 6806508 10534719 WO71 6810708 10534719 WO71 6824208 10534585 WO71 6801108 10534635 W07l 6802208 10534669 WO71 6796008 10534306 WO71 6799108 10534440 WO71 6199208 10534690 WO71 6800808 10534690 WO71 6616308 10534799 WO71 6826208 10534695 WO71 6811608 10534445 WO71 6812608 10534692 WO71 6812708 10534444 WO71 6812808 10534443 WO71 6812908 10534801 WO71 6813108 10534453 W071 6813208 10534697 WO71 6813308 10534451 WO71 6813408 10534696 WO71 6813508 10534694 WO71 6813608 10534698 WO71 6813708 10535136 WO71 6823308 10534416 WO71 6822908 10534778 WO71 6830909 10534104 W071 6810608 10537853 W071 6602508 10534307 W071 6808508
Whatman, Inc. is recalling Whatman Body Fluid Collection Paper 903 The device is used by healthcare professionals in the colle due to The two portions of the card are coming apart prematurely.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The two portions of the card are coming apart prematurely.
Recommended Action
Per FDA guidance
Whatman issued an Urgent Medical Device Correction letter to to the direct account on 5/6/09 requesting this notice is distributed to users. The notice states the safety issue; requests users to inspect 903 cards prior to use, if the 903 Paper Portion of the card partially or completely detaches from the Demographic portion of the card, discard the card obtain a new card and inspect. On May 26, 2009 the firm expanded the notification to additional users of the 903 cards to inspect cards prior to use.
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