Complete FDA and NHTSA recall records dated in April 2026.
These records include useful source details for the selected month.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or…
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or…
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or…
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or…
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or…
Contains undeclared egg, soy, and hazelnut
Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.
FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Potential Salmonella Contamination
Products contain banned sweetener: cyclamates.
FDA analysis revealed the presence of undeclared sildenafil
Products contain banned sweetener: cyclamates.
FDA analysis revealed the presence of undeclared sildenafil
Label declares cream cheese but does not declare milk
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
Lack of Assurance of Sterility
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
