BD Extension Sets Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
BD SWITZERLAND SARL is recalling 93,700 units of three intravascular administration and extension sets due to potential inadequate sterilization processing.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 26, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
BD SWITZERLAND SARL initiated a voluntary recall of certain intravascular administration sets and extension sets because the products may not have received adequate sterilization processing. The recall is classified as Class II.
Which Products Are Affected
The following products are affected:
- 60 In Non-DEHP Minibore Extension Set RES ME2010, UDI-DI code: 10885403236235, Lot Number: 26025260
- MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C, UDI-DI code: 10885403274619, Lot Number: 26035455
- 9 IN Extension Set w/Max Y REF MPX5300-C, UDI-DI code: 10885403237218, Lot Number: 26055528
A total of 93,700 units were distributed in the U.S. states of AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MO, MS, NC, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA and in Canada. Recall number Z-2941-2026.
What You Should Do
Consumers should stop using the affected products and contact the recalling firm for return or refund instructions.
Why This Matters
Inadequate sterilization processing of devices used to administer fluids poses a risk of infection.
Source
FDA recall Z-2941-2026, report date 20260819.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,143 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 26, 2026.
Frequently Asked Questions
Common questions about this FDA recall.