Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV…
The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
Read the official notice →- Date
- 2022-12-14
- Country
- United States
- Brand
- Medical Action Industries
- Product
- Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF…
- Classification
- Class II
- Units
- Distribution was made to MN. There was no foreign/government/military…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
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The kits contain saline flush syringes which were recalled by the supplier.
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Other drugs & medical recalls in the United States
- 2022-12-21
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Exela Pharma Sciences LLC recalls 8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd…
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- US
- 2022-12-14
- US
Arthrex, Inc. recalls Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a cannulated reamer, sterile.
The devices may be packaged with the wrong reamer size.
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Philips North America Llc recalls Philips SmartPath to Ingenia Elition X MR System, Model Numbers 782118, 782132, 782144
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Intersect ENT, Inc. recalls Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044
Sinus Implant product label displays incorrect product information including: "Straight Delivery System", with incorrect reference number and UDI-DI.
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Device exceeds the limitations of a Class I 510(k)-exempt device so the user manual, instructions for use, and promotional materials are being corrected to remove all references to downstream applications.