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…
Read the official notice →- Date
- 2026-08-26
- Country
- United States
- Brand
- American Contract Systems
- Product
- American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR CERVICAL PACK - 205988, Model Item Number MHAC65AH; 2)…
- Classification
- Class II
- Units
- US distribution to states of: MN, MO, IA
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 American Contract Systems recalls
- 2026-10-07
USAmerican Contract Systems Inc recalls Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL HYSTERECTOMY - 205989…
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FDA · DeviceAmerican Contract Systems IncUS Nationwide distribution in the states of Iowa, Minnesota, Wisconsin, and…Official notice →- 2026-09-02
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American Contract Systems Inc recalls American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H
The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable…
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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 → - 2026-05-13
- US
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 → - 2025-10-22
- US
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…
FDA · DeviceAmerican Contract Systems Inc.US Nationwide distribution in the states of SD, IA, MN, WA, IL.Official notice → - 2025-09-03
- US
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…
Other drugs & medical recalls in the United States
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- 2026-08-27
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Kmaier Recalls Infant Walkers Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers
The recalled walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall hazard.
- 2026-08-26
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restor3d Inc. recalls Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog Number: 1500-1030;…
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
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ConvaTec, Inc recalls Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710, 423712, 423713,…
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The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could result in an unreliable fault current return path.
FDA · DeviceFort Defiance Industries, LLCWorldwide - US Nationwide distribution in the states of MD, VA, NJ, TN and the…Official notice →