Stryker Sustainability Solutions recalls HoverMatt, 39" W x 78" L, REF: HM39SPU-B
39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide mattresses, so there may be a decreased surface area available to distribute the patient's weight across, which may increase the effort…
Read the official notice →- Date
- 2023-08-16
- Country
- United States
- Brand
- Stryker Sustainability Solutions
- Product
- HoverMatt, 39" W x 78" L, REF: HM39SPU-B
- Classification
- Class II
- Units
- US: WI, ID, CA, FL, HI, MD, RI, AZ, MA, GA, 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 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 Stryker Sustainability Solutions recalls
- 2024-08-28
USStryker Sustainability Solutions recalls Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5A
Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing,…
FDA · DeviceStryker Sustainability SolutionsUS Nationwide distribution in the states of FL, WY, AZ, CA, LA, TX, MI, OR,…Official notice →- 2024-07-24
- US
Stryker Sustainability Solutions recalls REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
FDA · DeviceStryker Sustainability SolutionsUS Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.Official notice → - 2024-07-10
- US
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions, BW Lasso 2515 NAV eco Variable Diagnostic EP Catheter, REF: D134301, ELECTRODES: 22,…
Diagnostic electrophysiology (EP) catheters do not meet testing requirements.
FDA · DeviceStryker Sustainability SolutionsInternational distribution to the country of Japan.Official notice → - 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.
- 2023-04-05
- US
Stryker Sustainability Solutions recalls Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single Bladder…
Increased incidence of disposable tourniquet cuffs "not able to achieve desired pressure" and "not holding pressure" due to 1) Cuff fabric tearing during use, and 2) Pinched or unseated O-ring at the connection between…
FDA · DeviceStryker Sustainability SolutionsUS: WI, MD, NY, PA, WA, CO, GA, FL, OH, NC, TX, NJ, OR, MT, CA, RI, SC, NE,…Official notice → - 2022-03-02
- US
Stryker Sustainability Solutions recalls REF: 5921-018-135, Stryker Color Cuff, 18" (Red), Quick Connect Single Port, Single Bladder
Mislabeling; dual-bladder tourniquet cuffs are labeled as single-bladder inflatable cuffs.
Other drugs & medical recalls in the United States
- 2023-08-23
- US
Colgate Palmolive Company recalls hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello…
Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon…
- 2023-08-16
- US
Philips North America recalls Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
During installation of the SmokeDetector Interlock, a connecting cable, between the SmokeDetector Interlock and the host PC, may not have been properly installed. This connection is used for service diagnostics and…
- US
Philips North America recalls Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
The system operator is able to bypass the SmokeDetector Interlock system locking mechanism after a smoke detection by power cycling the system.
- US
Cytrellis Biosystems, Inc. recalls ellacor System with Micro-Coring Technology-Indicated for use by medical professionals for the treatment of moderate and severe…
Potential failure of a bearing adhesive joint that can occur due to an assembly issue of the X/Y stage of the handpiece. If a broken glue bond were to occur, it could cause an overlap of cores, potentially leading to…
- US
Canon Medical System, USA, INC. recalls INFX-8000C XGCP-930AA TABLE SIDE CONSOLE, INFX-8000C XGCP-930BA TABLE SIDE CONSOLE
The C-arm, used to set the position and angle of the x-ray exposure field, may not function due to the tableside console PWB, which needs replacement. There may be a delay in the procedure, but procedures can continue…
FDA · DeviceCanon Medical System, USA, INC.US Nationwide Distribution: NY, CO, IL, CA, MD, MN, WAOfficial notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Total Hip Kit, REF DYNJ903275S; surgical convenience kit
The prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of Illinois.Official notice →