American Contract Systems, Inc. recalls BASIN SET, MEBS42K, general surgical kit
Basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.
Read the official notice →- Date
- 2022-11-30
- Country
- United States
- Brand
- American Contract Systems
- Product
- BASIN SET, MEBS42K, general surgical kit
- Classification
- Class II
- Units
- US Nationwide distribution.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2024-02-07
US
American Contract Systems, Inc. recalls Procedural convenience kits and trays, cardiac, labeled as: a) EP LAB BI V IMPLANT PACK, kit number AGBI64J; b) LAB DEVICE…
During an internal investigation, ACS identified that several components were "piggybacked" to ACS trays and subjected to the ACS sterilization process. There is no supporting documentation stating the "piggybacked"…
- 2023-11-01
US
American Contract Systems, Inc. recalls LAVH, REF BBLV21C
During an internal investigation, ACS identified that the components, I.V. Cath (part number 4252535-02) and Adhesive Dermabond (part number DHVM12) were inadvertently subjected to the ACS sterilization process and…
FDA · DeviceAmerican Contract Systems, Inc.US Nationwide distribution in the states of FL, IA.Official notice →- 2023-06-21
US
American Contract Systems, Inc. recalls Total Knee Pack, REF CETJ130, medical convenience kits
Incorrect expiration date on product.
- 2022-10-19
US
American Contract Systems, Inc. recalls COVID Test Kit Nonsterile
Kit incorrectly labeled for use with COVID testing and should not be used with any SARS-Co-V2 device.
- 2022-09-14
US
American Contract Systems, Inc. recalls Various Angiography packs/trays
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
FDA · DeviceAmerican Contract Systems, Inc.Distribution within the United States to health systems and distributors in…Official notice →- 2022-07-13
US
American Contract Systems, Inc. recalls Clean Catch Urine Kit NS 178489, AHMU58A
Affected products were assembled off-site by individuals who may not have been properly trained.
FDA · DeviceAmerican Contract Systems, Inc.US distribution in the state of Minnesota.Official notice →
Other drugs & medical recalls in the United States
- 2022-11-30
US
US
Southmedic, Inc. recalls Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO
Upon review of its batch record, Southmedic identified that lot # W92761 was not sent out for sterilization, and was instead transferred directly to distribution where it was sold and distributed to customers as…
US
Pajunk Medical Systems, L.P. recalls PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model #TAL101,…
The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml ampule of 0.9% Sodium Chloride as intended,.
FDA · DevicePajunk Medical Systems, L.P.US Nationwide distribution in the states of CA, NC, TN, PA, and TX.Official notice →US
Corin Ltd recalls Unity Total Knee System. Used for knee prosthesis in total knee replacement
The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging.
FDA · DeviceCorin LtdDistribution in the US to New Jersy and Puerto Rico. International…Official notice →US
Smiths Medical ASD Inc. recalls Medfusion Model 4000 Syringe Infusion Pump, with software versions V1.6.0 or V1.6.1 that have implemented the Smart Pump Programming…
Potential for delay in sending Infusion Start Messages to third-party Electronic Health Record systems which may affect infusion auto-programming on the pump and documentation
FDA · DeviceSmiths Medical ASD Inc.US distribution to states of: Indiana, Texas and VirginiaOfficial notice →US
Kamiya Biomedical Company, LLC recalls K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013
IgA Reagent may start showing cloudiness over time, which can affect assay performance.
FDA · DeviceKamiya Biomedical Company, LLCWorldwide - US Nationwide distribution in the states of FL, NC, TX, TN, PA,…Official notice →