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All product recalls associated with Oasis Medical Inc.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
"Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues additional products are now being classified by the agency". Foreign deposit present on the surface of the Vidaurri LASIK Flap Irrigators
The product valve has a high probability of deforming and may result in leakage during use.
These 5-foot-tall Tiki® bamboo torches consist of a bamboo pole with a weaved basket at the top and a metal flame guard, which is a circular black piece that holds the wick in place and attaches to the fuel canister. The recall includes the Tiki® Beachcomber, Seagrass and Sandpiper model torches. The recall also involves replacement canisters that have the metal flame guards. Recalled units have the following UPC numbers: 086861010372 (Beachcomber), 086861013335 (Seagrass), 086861010457 (Sandpiper) and 076354995262 (Replacement Canister). The UPC number and the model name are written on the packaging or attached tag.
The recall includes toy boxes with manufacture date codes between November 2002 and July 2004 and the following model numbers and colors: 01520-331 - white, 01520-334 - cherry, 01520-33C - cognac, 01520-33L - oak, and 01520-33N - natural. The manufacture date codes, model numbers, and colors are located on a label underneath the toy boxes. The toy boxes measure 27 inches long by 18 inches wide and 17 inches high. The boxes are constructed of pine.
During use of GE Signa nuclear magnetic resonance imaging system, a flexible Teflon tube that was part of the magnet vent system ruptured and allowed the magnet to vent into the scan room. Because of helium pressure inside the room, the scan room door could not be reopened after the patient was removed from the scan room.
GeoDeck™ is a composite decking product that looks similar to natural wood and is sold in three colors, including: driftwood, cedar and mahogany. The decking materials were manufactured between April 2002 and October 2003. Each decking and railing component has a manufacturing date stamp (day/month/year) on the cut end, which may still be visible on uninstalled materials.
The image balance center point correction algorithm used in CT image reconstruction may cause a disapperance or alteration of small circular anatomical structures that are both near the image center and perpendicular to the image plane. This artifact may lead to the misinterpretation of anatomy at the center of the image.
This recall involves Torelli Verona and Lugano Open Tubular bicycle tires with folding Kevlar beads, used to hold the tire to the rim. A red and white label on the sidewall of the Verona model has "Torelli Verona 700 X 23 100-130 psi Handmade Open Tubular" printed on it. A green and white label on the lower edge of the Lugano model has "Torelli Lugano 700 X 23 100-130 psi Handmade Open Tubular" printed on it. The tires are packaged in red and white boxes with the Torelli logo on the front.
Critically ill patients undergoing continuous renal replacement therapy may suffer excessive fluid loss.
The above wheels were sold by Ritchey as wheel sets and as rear wheel only and as original equipment on 2004 model year Fuji and Motobecane USA bicycles and the 2005 model year Prestige road bike from Raleigh. The recalled wheels have high flange hubs measuring 60 milimeters in diameter and the hub body is straight between the flanges.
The recalled strollers have an aluminum frame and a cloth seat with a sun canopy. The recalled single seat Speedster Deluxe stroller has model number 20050116 and serial numbers: S2000001D0504 through S2000500D0504 and S2000001D0505 through S2000100D0505. The recalled double seat Speedster Deuce Jogging strollers have model number: 20050216 and serial numbers: S3000001D0504 through S3000300D0504 and S3000001D0505 through S3000075D0505. Each stroller has a tag, located inside the child's seat compartment, which lists the model name and model number. A sticker on the rear frame lists the serial number.
Invitro diagnostic test kit used for testing to confirm the presence of tuberculosis contains interfering bioburden which can cause false positive results.
False Positive results may be obtained with the identified lot of list 3A60-16 when using a negative patient sample or a negative control.
Phototherapy medical device may lose its position and can cause a safety hazard to the patient.
Through the complaint handling system, the company has determine there are performance issued involving the LS7500, 300 Watt Xenon Light Source. The performance issues result in a low light output that can create poor illumination of the surgical site.
The tube clamp mechanism on the roller pump may not open when the rotation knob is turned, making it difficult to remove and/or insert tubing.
The power supply may fail to function due to a defective capacitor. (Note; this device incorporates a redundant separate power supply not affected by this capacitor)
The recall includes model year 2005 Polaris "900 Fusion," "900 RMK," and "900 Switchback" snowmobiles with model numbers: S05PL8DSD, S05PM8DS(A)(B), S05PN8DS, S05PS8DS, S05PM8DS(A)(B)(C), S05PL8DS(A)(B)(C). The snowmobile model and serial number identification decal is located on the right-front side decal of the tunnel. The serial number is permanently stamped into the tunnel and the model number is embossed on the decal.
Serum Blood Collection tubes found with excess of Blood Clot Accelerator (BCA) solution.
Biliary Stents may malfunction and cause failure to expand, fracture, incomplete deployment, inaccurate positioning, migration, or lumen perforation.