CareFusion 303, Inc. recalls Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to x.x.x.255
Infusion pump PCs with specific software/network cards/IP addresses can have network/wireless connection failure. Could cause inability to receive new datasets and inability to transfer retrospective analytics data to…
Read the official notice →- Date
- 2023-03-08
- Country
- United States
- Brand
- CareFusion
- Product
- Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to x.x.x.255
- Classification
- Class II
- Units
- US: FL, CA, OR, IL, WI, NJ, AZ, NV, CO, WY, NE, TX, MI, VA, OH, NC, LA, NM,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More CareFusion recalls
- 2023-05-03
USCarefusion 2200 Inc recalls (1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2) Carefusion V. Mueller…
A portion of the two products were incorrectly marked (etched) and packaged resulting in a product mismatch. The labels and laser etchings were switched on the two products.
FDA · DeviceCarefusion 2200 IncDistribution was made to AL, AR, AZ, CA, CO, CT, FL, HI, IA, IL, IN, KY, LA,…Official notice →- 2023-03-29
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Automated dispensing cabinet drawer firmware may have inadvertently been downgraded to an earlier version of drawer firmware during new device installations or device replacement upgrades, which may lead to an…
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Product did not meet shelf-life testing requirements resulting in a breach of the sterility of the Genesis container holding surgical equipment.
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FDA · DeviceCareFusion 303, Inc.U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CO,…Official notice → - 2022-12-14
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Carefusion 2200 Inc recalls CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2" (240MM) , REF F-5008
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FDA · DeviceCarefusion 2200 IncNationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines,…Official notice → - US
Carefusion 2200 Inc recalls Carefusion V. Mueller" CUSHING BAYONET BIPOLAR FORCEPS, 2.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-2004
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Other drugs & medical recalls in the United States
- 2023-03-08
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Beaver Visitec International, Inc. recalls Ultracell Wick with 80cc Collection Bag, 20/box
Device packaging may contain open seals, compromising product sterility.
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CooperVision, Inc. recalls Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)
Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
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Unetixs Vascular, Inc. recalls MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01
The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
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Stryker has identified a nonconformance in specific lots of Hoffmann LRF Bone Transport Struts. Specifically, the thread pitch is oversized at the distal end of the threaded rod, and as a result the distal ring…
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Maquet Medical Systems USA recalls BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code 70106.9077, BEQ-HLS 7050 USA; HLS Set Advanced 7.0, Product Code 70106.9078.…
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Encore Medical, LP recalls EMPOWR VVC KNEE TIBIAL INSERT, SIZE 6, 22MM, REF: 346-22-706; EMPOWR VVC KNEE TIBIAL INSERT, SIZE 7, 22MM, REF: 346-22-707; EMPOWR VVC…
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