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.
Read the official notice →- Date
- 2024-05-01
- Country
- United States
- Brand
- 3M Company - Health Care Business
- Product
- 3M Durapore Surgical Tape, Catalog Number 1538-118
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide in the states of TX, NY, NH, AZ, NC,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2025-01-01
US3M Company - Health Care Business recalls Clarity Precision Grip Attachments, for use in orthodontic treatment. Part numbers/SKUs: 359-830 359-831 359-832 359-833…
Attachments may not mate with the tooth as intended in the digital treatment design.
FDA · Device3M Company - Health Care BusinessProduct was distributed nationwide US, and internationally to Canada,…Official notice →- 2024-10-16
- US
3M 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 → - 2024-04-10
- 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 → - 2023-05-24
- US
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.
FDA · Device3M Company - Health Care BusinessWorldwide distribution: US (nationwide) and OUS (foreign) countries of:…Official notice →
Other drugs & medical recalls in the United States
- 2024-05-01
- US
Electro Medical Systems SA recalls Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number: EG-121 Software Version: N/A Product Description: These…
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the…
FDA · DeviceElectro Medical Systems SAWorldwide distribution - U.S. Nationwide in the states of IL and TX. The…Official notice → - US
Quidel Corporation recalls QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests
There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test results, the positivite test line may…
FDA · DeviceQuidel CorporationUS: AK AL AR AZ CA CO CT DC FL GA HI IA ID IL IN KS KY LA MA MD MI MN MO MT NC…Official notice → - US
Covidien LP recalls Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm) x 19 cm (Symmetrical Tip, Heparin Coating, Silver Ion Sleeve and…
Products may not be heparin coated as indicated on the label-leads to a potential loss of benefit due to the absence of the heparin coating
FDA · DeviceCovidien LPWorldwide distribution - US Nationwide and the countries of Austria, Belgium,…Official notice → - US
Howmedica Osteonics Corp. recalls TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
FDA · DeviceHowmedica Osteonics Corp.Nationwide Foreign: Netherlands, Canada, Singapore, Spain, Sweden, UKOfficial notice → - US
SEASPINE ORTHOPEDICS CORPORATION recalls Mariner RDX MIS Polyaxial Head, REF: MX1-001010, part of Mariner RDX MIS Alpha Instruments and Implants, REF: AMRDXMIS, which…
Screw heads, of pedicle screw systems, have partial thread within the screw head that pose a risk of intraoperative cross-threading within the locking cap/screw head interface.
- US
EBI, LLC recalls 48" Lead Wires, Replacement Part Number: 1067724-4
Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment