Loading...
Loading...
All product recalls associated with ConvaTec.
Total Recalls
1000
Past Year
123
Class I (Serious)
69
Most Recent
Nov 2025
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.
Cartons labeled 1-1/4 inch size may contain units that are 1-1/2 inch size.
The recall involves some X650 second stage regulators. All X650 second stage regulators are clearly marked with a blue capital "X" next to the numbers "650" in white. Affected regulators have a visible bump located on the right side of the unit between the letter "C" and where the mouthpiece attaches to the regulator body.
The 9F device may contain a 10 F sheath instead of the 9F
The 9F device may contain a 10 F sheath instead of the 9F
The 9F device may contain a 10 F sheath instead of the 9F
Potential for patient waveforms to move to an open receiver module or to an occupied receiver causing the intermittent inappropriate monitoring of both patients for several minutes.
The recalled helmets are identified by the model name Anthem C Elite and Anthem C Elite WSD. A label inside the helmet identifies the helmet as "Trek Anthem C." The helmets are available in men's sizes in black/charcoal, blue/silver and blue/red, and in women's sizes in aqua blue/silver and white/silver. This recall includes all sizes of this helmet.
THE ARTICULATING ARM ON THE CART, WHICH HOLDS THE MONITOR, MAY FALL OFF FROM THE CART DURING MANIPULATION. WHEN IT FALLS, IT COULD HIT THE GROUND OR FALL ON THE PEOPLE/OBJECTS THAT ARE IN CLOSE PROXIMITY.
The end label on the outer box was mislabeled on 9 of a 10 unit lot. The end label says ''22 mm'' and the implants are actually ''20 mm''. The main label on the cardboard box applied by the contract packager is correct in identifying the product as ''20 mm''.
The Sternum Saw Collet Nut that is used to insert and hold the saw blade in place may not always allow for the easy insertion of a saw blade into the handpiece for use. The nut needs to be in a certain position in order for the blade to be inserted and this may delay the operation of the device especially in emergency situations.
The immersion heaters are portable chrome-plated steel heaters with a white plastic handle and mug hook used for warming tea, coffee, soup, or other liquids. "IMMERSION HEATER," and "MADE IN TAIWAN" are embossed on the white plastic handle of these heaters. Some products were sold under the EKCO brand and others were sold with no brand.
Potential for incorrect weight to be displayed.
The recall involves 75-gallon propane gas water heaters. The heaters have the name "A.O. Smith," "Reliance," "Apollo," "State," or "Maytag" on the side of the unit. The model number is located on the rating plate. Only units with the model numbers listed below and manufactured between January 2004 and July 2005 are included in the recall. Brand Name Model Number Reliance 675CRRS 675CRRSD S7576PE Apollo A675CQRSL A675CRRSL A675CRRSLCGAD A. O. Smith BT-80-271 FCG-75-271 PCG-75-271 Maytag HRP11275Q State GS675CRRS GS675CRRSD SBS7576PE SBS7576PED SBS7576PECGA SBS7576PECGAD If your unit has one of the model numbers listed above, locate the serial number on the rating plate to determine if it was manufactured between January 2004 and July 2005. If your unit has one of the model numbers listed above, locate the serial number on the rating plate to determine if it was manufactured between January 2004 and July 2005. The serial numbers of units manufactured between January 2004 and July 2005 are listed below. Month/Date of Manufacture Serial Number Begins With: Jan-04 MA04 or AA04 or A04 Feb-04 MB04 or AB04 of B04 Mar-04 MC04 or AC04 or C04 Apr-04 MD04 or AD04 or D04 May-04 ME04 or AE04 or E04 Jun-04 MF04 or AF04 or F04 Jul-04 G04 Aug-04 H04 Sep-04 J04 Oct-04 K04 Nov-04 L04 Dec-04 M04 Jan-05 A05 Feb-05 B05 Mar-05 C05 Apr-05 D05 May-05 E05 Jun-05 F05 Jul-05 G05
Two conditions may occur with the S/5 Aespire Anesthesia System. The internal auxiliary flowmeter tubing may become disconnected if the auxiliary oxygen supply tubing is occluded and the patient may not receive desired supplemental oxygen which could lead to serious injury if undetected. Also the O2 switch may leak or fail.
Two conditions may occur with the S/5 Aespire Anesthesia System. The internal auxiliary flowmeter tubing may become disconnected if the auxiliary oxygen supply tubing is occluded and the patient may not receive desired supplemental oxygen which could lead to serious injury if undetected. Also the O2 switch may leak or fail.
ECG 5-lead cable miswired - A physician could interpret the incorrect polarities as a conduction defect.
The footswitch may develop a system fault resulting in the self-activation of the handpiece it controls, or it may cause the handpiece to run intermittently or to revert to a default setting.
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 transducer used to compensate for pressure changes was mounted backwards on the printed circuit board assembly. The module will not compensate for pressure changes and CO2 readings will be inaccurate at higher altitudes.