3M Company - Health Care Business recalls 3M Attest Steam Chemical Integrators, REF 1243B
3M Attest Steam Chemical Integrators with dates of manufacture between November 6, 2022 and January 17, 2023 have an increased potential to leak ink during a sterilization cycle.
Read the official notice →- Date
- 2023-05-24
- Country
- United States
- Brand
- 3M Company - Health Care Business
- Product
- 3M Attest Steam Chemical Integrators, REF 1243B
- Classification
- Class II
- Units
- Worldwide distribution: US (nationwide) and OUS (foreign) countries of:…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 3M Company - Health Care Business recalls
- 2024-10-16
US3M Company - Health Care Business recalls 3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R
Contamination with foreign substance matter
FDA · Device3M Company - Health Care BusinessInternational distribution to the country of South Korea.Official notice →- 2024-05-01
- US
3M Company - Health Care Business recalls 3M Durapore Surgical Tape, Catalog Number 1538-118
Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were incorrectly labeled with a shelf life of 5 years, rather than 3 years.
FDA · Device3M Company - Health Care BusinessWorldwide distribution - US Nationwide in the states of TX, NY, NH, AZ, NC,…Official notice → - 2024-04-10
- US
3M Company - Health Care Business recalls 3M Tube Securement Device, Small, 1.7 IN/PO x 2.4 IN/PO, REF 1500U, Sterile; and 3M Tube Securement Device, Large, 2.2 IN/PO x…
Manufacturing nonconformities are in some lots of the Tube Securement Device, such as the top film layer may be partially or completely missing and some devices may exhibit the appearance of an incorrect shape due to…
FDA · Device3M Company - Health Care BusinessWorldwide distribution - US Nationwide distribution in the states of CA, CO,…Official notice → - 2024-02-28
- US
3M Company - Health Care Business recalls 3M Specialty Blade Assembly, REF 9660,70-2011-8462-2, 7100213114, used with used with 3M Surgical Clipper Catalog Number 9661L
3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in minor injury: " Do not use on injured skin. " Do not leave…
- 2023-10-04
- US
3M Company - Health Care Business recalls 3M Attest Super Rapid Readout Biological Indicator, REF 1492V; used to qualify or monitor dynamic-air-removal steam…
Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam Challenge (1496V) may contain…
FDA · Device3M Company - Health Care BusinessWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice → - 2021-11-10
- US
3M Company - Health Care Business recalls 3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape, Catalog No. 2244, (3M ID (SKU): 70-2011-8506-6, SAP ID:…
Potential for breakage of the ECG electrode carbon stud from the eyelet.
FDA · Device3M Company - Health Care BusinessUS Nationwide Distribution to states of: AL, AZ, CA, IA, IL, LA, MD, MO, NC,…Official notice →
Other drugs & medical recalls in the United States
- 2023-05-31
- US
Central Admixture Pharmacy Services, Inc. recalls vasopressin 20 units added to 0.9% sodium chloride 100 mL*, 0.2 units/mL*, 100 mL per bag, Rx only, Central Admixture…
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
- 2023-05-24
- US
Stryker Sustainability Solutions recalls REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile
Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be mislabeled and/or mispackaged.
- US
TELEFLEX LLC recalls Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue tracts of femoral…
The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the product.
- US
Beckman Coulter Inc. recalls Beckman Coulter Bicarbonate, REF: OSR6137, 4x25 mL
There is a potential for a decrease in calibration ODs for Bicarbonate reagent which could result in calibration failures and/or quality control failures.
FDA · DeviceBeckman Coulter Inc.Worldwide Distribution: US (nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, DE,…Official notice → - US
Access Vascular, Inc recalls HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package.
- US
Hiossen Inc. recalls ET III Nano-HA fixture System ET NH Dental Implant Model # ET3R5010B -Intended for Dental Implant Catalog #: AET3R5010B
Mis-labeled length of the dental implant on the Recall Implant's package. Dental implant size D5.0 x L8.5mm, labeled as D5.0 x L10mm