MEDLINE INDUSTRIES, LP - Northfield recalls Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS
Medline is recalling certain lots of our Adult Portable Bed Rails that were manufactured after the mandatory compliance requirement (ASTM F3186-17, Standard Specification for Adult Portable Bed Rails and Related…
Read the official notice →- Date
- 2024-04-17
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the country of Canada.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 MEDLINE INDUSTRIES, LP - Northfield recalls
- 2024-06-05
USMEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PUDENDAL…
Trumpet Needle Guide ring can detach when excessive pressure is applied.
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) REF DYNJ18860, Polyurethane Cuff 6.0 mm ID; (2) REF…
Complaints have been received that the device inflation tube detached and/or tore from the main tube, resulting in potential moisture buildup, loss of pressure, or inability to inflate. There were also reports the…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistribution was nationwide. There was government/military distributon.…Official notice → - 2024-05-22
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Namic FLUID DELIVERY SET, REF 91300040
Products have a lack of sterility assurance.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AL, FL, KY, MS, TX, WA, WI, NC,…Official notice → - 2024-04-10
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Blood Pressure Unit, Model (REF) Numbers: a) MDS4001, b) MDS4001LA, c) MDS4001PLUS
The firm provided a set of specifications for the device, but some units of the device were manufactured non-compliant with the specifications. However, the firms Receiving Dept. accepted these units into inventory
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion manual surgical kits labeled as: a) STERILE 4-1/2" S/S SCISSOR (SS5031), Product Code 65145; b) STERILE S/B…
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Panama, Canada.Official notice → - 2024-03-20
- US
MEDLINE INDUSTRIES, LP - Northfield recalls CVS Health Waterproof Wound Tracking Dressing, REF CVS690330, immediate package contains 1 sterile dressing, 4 in. x 4 in.,…
Product failed sterility testing.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AL, CA, FL, IN, MI, MO, NJ, NY,…Official notice →
Other drugs & medical recalls in the United States
- 2024-04-17
- US
Synovo Production recalls Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V ELI, TiN CERAMIC W/ PLASMA SPRAY, STERILEEO, Reference Numbers: 01-03-0042 01-03-0044…
Medical device components were marketed without FDA clearance
- US
Synovo Production recalls ACETABULAR FIXATION CUP, (xx)MM, 5 HOLE, Ti-6AI-4V ELI TiN CERAMIC W/PLASMA SPRAY, STERILEEO, Reference Numbers: 01-01-0554 01-01-0556…
Medical device components were marketed without FDA clearance and without FDA approval
- US
ConvaTec, Inc recalls ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1 dressing/immediate package, 5…
The product does not meet sterility assurance level.
FDA · DeviceConvaTec, IncUS Nationwide distribution in the states of CA, MO, NM, PA, TX, and WA.Official notice → - US
Human Care Hc Sweden Ab recalls Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient lifts
Patient lift hanger bar may come loose, which could potentially pose risks to patients.
FDA · DeviceHuman Care Hc Sweden AbUS Nationwide distribution in the states of TX, IL, OK, CA.Official notice → - US
Fresenius Kabi USA, LLC recalls LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0.
Software has anomalies that have the potential to cause underdose, overdose, or delay in therapy which could lead to serious patient harm or death.
FDA · DeviceFresenius Kabi USA, LLCUS Distribution: CA, CO, ID, MI, NE, NJ, NV, OK, TX, UT, VA, WA, & WI.Official notice → - US
Microbiologics Inc recalls KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b, a) REF 0209P and b) REF 0209K, Quality control kit for culture media
The positive control material (Rhizopus stolonifer) within the KWIK-STIK assembly was contaminated with another fungal organism (Aspergillus brasiliensis). As a result, users may observe A. brasiliensis growth when…
FDA · DeviceMicrobiologics IncWorldwide - US Nationwide distribution in the states of CA, MI, KY, MO, NM,…Official notice →