FDAJune 21, 2021device
DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842072 d) REF 3852072
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
What to do
FDA enforcement status: Ongoing
Brands named
delta med spadeltadelta med
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCSpa Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Arrogantf2026-06-18
- FDAAdvance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-282026-05-27
- CPSCEcoFlow Technology Recalls Delta Max 2000 Power Stations Due to Risk of Serious Burn Injury and Fire Hazard2025-10-09
- CPSCPeg Perego Recalls Tatamia 3-in-1 Recliners, Swings and High Chairs Due to Risk of Suffocation; Violations of Multiple Federal Standards (Recall Alert)2025-06-26
- CPSCDelta Gas Ball Valves Recalled Due to Fire and Burn Hazards; Manufactured by Masco Canada2025-05-08
- FDADORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)2025-03-14
- FDAProduct is a whole, fresh cucumber with no individual packaging, labeling, PLU, or other identifying information. Cucumber weight and size varies. Type of master packaging: 1.PACKAGED IN BULK IN 1 1/9 BUSHEL CARDBOARD BOXES WITH THE DELTA FRESH LABEL; OR 2.PACKAGED IN BULK IN 1 1/9 BUSHEL GENERIC...2024-11-27
- FDASUC-4300S, Rigid Intracardiac Sucker Fluted Tip; 1/4" (6.4mm) connector 13" (33cm) length. Indicated for handheld use only to remove excess fluid from the surgical field.2024-11-19
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