Drugs & medicalClass II

Allison Medical, Inc. recalls InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC

Insulin syringe retail packages incorrectly labeled as "Short Needle".

Read the official notice →
Date
2022-11-30
Country
United States
Brand
Allison Medical
Product
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Classification
Class II
Units
Texas
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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 Allison Medical recalls

  1. 2022-12-21
  2. US
    Drugs & medicalClass II

    Allison Medical, Inc. recalls CarePoint 60 mL Syringe Without Needle, REF: 04-7560

    Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown.

    FDA · DeviceAllison Medical, Inc.US: IA, LA, MS, FL, PR; OUS: BARBADOSOfficial notice →
All 2 Allison Medical recalls →

Other drugs & medical recalls in the United States

  1. 2022-11-30
  2. US
    Drugs & medicalClass II

    Beckman Coulter, Inc. recalls MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280

    Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect diffuser plate.

    FDA · DeviceBeckman Coulter, Inc.Worldwide - U.S. Nationwide distribution in the states of AK, FL, IA, ID, MI…Official notice →
  3. US
    Drugs & medicalClass II

    Abbott Molecular, Inc. recalls Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use

    Abbott has identified potential performance issues for the Alinity m System software version 1.6.5: 1) In a unique scenario, the waste chute flapper was found to not open when the Systems Solution drawer was closed and…

    FDA · DeviceAbbott Molecular, Inc.Worldwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    Hamilton Medical AG recalls Hamilton-C6

    Due to a malfunction related to the backlight on the ventilator screen. The screen goes black for approximately 2-3 seconds, but it brightens up again when the backlight switches on again.

    FDA · DeviceHamilton Medical AGU.S. Nationwide distribution including in the states of CA, FL, GA, ID, IN,…Official notice →
  5. US
    Drugs & medicalClass II

    Medical Action Industries, Inc. 306 recalls B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected…

    The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.

    FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the state of Pennsylvania.Official notice →
  6. US
    Drugs & medicalClass II

    3M Healthcare Business recalls 3M Steri-Drape, Small Drape with Adhesive Aperture, REF 1020, general surgery drape

    During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product unusable. Additionally, 3M has…

    FDA · Device3M Healthcare BusinessWorldwide distribution.Official notice →
  7. US
    Drugs & medicalClass I

    Whele LLC DBA Perch recalls Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 ) Blue Electric Heating Pad, MB-002

    The products may have the potential to burn customers. Firm has received complaints of burns, mild shocks, and rashes/irritation.

    FDA · DeviceWhele LLC DBA PerchUS Nationwide through Amazon.com and Walmart.Official notice →
See all drugs & medical recalls →