Bd Switzerland Sarl recalls
9 recalls in our records from 2020 to 2026: 9 FDA medical devices.
Recalls with full detail pages
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Bd Switzerland Sarl medical device recall: BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563…
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.
Earlier and other recalls
These link to the official agency notice.
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Bd Switzerland Sarl medical device recall: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code:… Official notice ↗
Products may not have received adequate sterilization processing.
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Bd Switzerland Sarl medical device recall: MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555… Official notice ↗
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
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Bd Switzerland Sarl medical device recall: BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106… Official notice ↗
Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This…
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Bd Switzerland Sarl medical device recall: BD PhaSeal Injector Luer Official notice ↗
Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare…
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Bd Switzerland Sarl medical device recall: Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded… Official notice ↗
Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer…
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Bd Switzerland Sarl medical device recall: BD Connecta BD Luer-Lok 360 Official notice ↗
Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU)
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Bd Switzerland Sarl medical device recall: Alaris Pump Infusion Set Low Sorbing Tubing Official notice ↗
Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.
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Bd Switzerland Sarl medical device recall: BD Alaris PCEA Administration Set Official notice ↗
The products have the potential to leak between the connection of the male luer and the yellow striped tubing. This leak may be observed while priming or during use. The…
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.