FDAJune 21, 2021device
NEO DELTA Self Safe 1, I.V. Catheter with PUR REF 3708122, Lot 00A1160627 5000 units
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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