New Jersey recalls

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Sedecal notified users that the Model 40KW-FX.899 mobile X-ray system is not water-resistant and must be cleaned exactly according to the manual instructions. Improper cleaning could damage the equipment.

Sedecal reminded users that its 40KWFX mobile X-ray systems are not water-resistant and must be cleaned strictly according to the manual instructions. Improper cleaning could damage the equipment. This notice affects 55 units distributed in California, Illinois, and New Jersey.

Sedecal is reminding users that the MobileDiagnost wDR 2.2 mobile X-ray system is not water-resistant. Improper cleaning can damage the equipment and may affect its safety and performance. Users must follow the cleaning instructions in the equipment manual.

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Unauthorized actors accessed product service credentials used by some BD technical support teams. This creates a risk that diagnostic test data and system information could be accessed, changed, or made unavailable until BD updates these credentials.

Unauthorized actors gained access to service credentials used by BD technical support teams to access the BD Phoenix M50 Automated Microbiology System. Until these credentials are updated, there is a risk that unauthorized individuals could access the system and view, modify, or disrupt patient data and system function.

Support service credentials for some BD MAX diagnostic systems were accessed by an unauthorized person. Until BD updates these credentials, there is a risk that someone could gain unauthorized access to the system and the data it contains.

Unauthorized actors gained access to service credentials used by BD technical support teams for the BACTEC 9120 blood culture system. Until credentials are updated, there is a risk that unauthorized parties could access the system or associated patient data.

Unauthorized actors accessed service credentials used by BD technical support teams to maintain certain BACTEC blood culture instruments. This could allow unauthorized access to affected devices and the patient data they contain until BD updates these credentials.

Service credentials used by BD technical support teams were accessed by an unauthorized person. Until BD updates these credentials, there is a risk that someone could gain unauthorized access to the system and its data.

Medline Industries identified a limited quantity of prefilled saline flush syringes (0.9% Sodium Chloride Injection, USP, 10 mL) that may not contain the correct concentration of sodium chloride. The affected syringes were distributed nationwide in the US and Canada.

Some Welch Allyn SureTemp Plus thermometer oral probes were incorrectly programmed with rectal probe settings. These affected probes may display temperatures that are lower than actual body temperature, which could delay treatment of fever or infection.

Tandem Diabetes Care insulin pumps (t:slim X2 and Mobi models) with certain software versions may deliver an unexpected automatic insulin correction dose when paired with a Dexcom G7 sensor. This could cause low blood sugar (hypoglycemia). The issue affects specific software versions: t:slim X2 versions 7.9.0.1 and 7.10.1, and Mobi version 7.9.0.1.

Product contains undeclared egg, FD&C Yellow 5, and FD&C Yellow 6.

Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes

Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes

Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.

Possible presence of stones in product

Possible presence of stones in product

Possible presence of stones in product