Drugs & medicalClass II

American Contract Systems Inc. recalls Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W ANGIOGRAPHY PACK MHCA98AK CORONARY ANGIO PACK- 205991…

Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to…

Read the official notice →
Date
2025-10-22
Country
United States
Brand
American Contract Systems
Product
Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W ANGIOGRAPHY PACK MHCA98AK CORONARY ANGIO PACK- 205991 RCAN45C…
Classification
Class II
Units
US Nationwide distribution in the states of SD, IA, MN, WA, IL.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 American Contract Systems recalls

  1. 2026-09-02
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    American Contract Systems Inc recalls American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN

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    FDA · DeviceAmerican Contract Systems IncUS Nationwide distribution in the states of IA, OH.Official notice →
  3. 2026-08-26
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    American Contract Systems Inc recalls American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR CERVICAL PACK - 205988, Model Item Number…

    The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected…

    FDA · DeviceAmerican Contract Systems IncUS distribution to states of: MN, MO, IAOfficial notice →
  5. 2026-05-13
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    American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers…

    Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential…

    FDA · DeviceAmerican Contract Systems IncUS distribution to MN. No OUS distribution.Official notice →
  7. 2025-09-03
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    American Contract Systems Inc recalls AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ANTERIOR HIP PACK, MODEL/ITEM NUMBER AMAH40N; 2)TOTAL…

    During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS…

    FDA · DeviceAmerican Contract Systems IncUS distribution to states of: IL and LAOfficial notice →
  9. 2025-06-18
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    American Contract Systems, Inc. recalls LOWER EXTREMITY, Model: NCEX20I; LOWER EXTREMITY, Model: NCEX20J; TOTAL KNEE PACK, Model: NCTK31K; TOTAL KNEE PACK, Model:…

    Test results for cast padding component included in procedure trays shows Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals exceeded residual limits, which may lead to a possible loss or lack of functionality…

    FDA · DeviceAmerican Contract Systems, Inc.US Nationwide distribution in the state of CO.Official notice →
  11. 2025-04-02
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    American Contract Systems, Inc. recalls Brand Name: Banner University Med Ctr. Product Name: Cardiac Cath Lab Pack-170278 Model/Catalog Number: GSCC40G Software…

    Sterility assurance with procedure trays

    FDA · DeviceAmerican Contract Systems, Inc.US: AZ OUS: NoneOfficial notice →
All 22 American Contract Systems recalls →

Other drugs & medical recalls in the United States

  1. 2025-10-29
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    The Harvard Drug Group LLC recalls Gabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack), Rx only, Packaged and Distributed by: Major Pharmaceuticals,…

    Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .

    FDA · DrugThe Harvard Drug Group LLCUS Nationwide.Official notice →
  3. 2025-10-22
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    Diagnostica Stago, Inc. recalls Product: STA Liatest D-Di; REF: 00515;

    A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.

    FDA · DeviceDiagnostica Stago, Inc.Worldwide distribution- US Nationwide and the country of Canada.Official notice →
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    Baxter Healthcare Corporation recalls CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve, 10 drops/mL, 92-inch (2.3 meters), Product code 2C8419

    IV sets may leak.

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    Spacelabs Healthcare, Inc. recalls Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01 Software…

    Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of…

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    Philips North America recalls Cardiac Workstation 5000; Model Number: 860439;

    Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.

    FDA · DevicePhilips North AmericaUS Nationwide distribution in the states of CA, IA, TN, TX, VA.Official notice →
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    ConvaTec, Inc recalls DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly exudating wounds.…

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