Manufacturer
341 recalls in our database name Covidien, LLC as the manufacturing or recalling firm.
Of the 341 recalls from Covidien, LLC we have scored against our rubric, 4 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 111 (33%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
FDA is recalling specific lots of Castile soap towelettes used in medical kits due to bacterial contamination.
FDA is recalling 10,000 units of Aplicare Castile Soap towelettes found in medical kits due to bacterial contamination.
FDA is recalling 300 units of Foley catheter trays containing bacteria-contaminated Castile soap towelettes. The product was distributed in the US and Canada.
Aplicare Castile Soap towelettes found in Foley trays and specimen kits are being recalled because they are contaminated with bacteria.
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
The FDA is recalling Aplicare Castile Soap towelettes included in Foley trays and midstream specimen kits due to bacterial contamination.
Castile soap towelettes in Foley trays and specimen kits are recalled because they are contaminated with bacteria.
FDA is recalling Castile soap towelettes in Foley trays and specimen kits due to bacterial contamination.
FDA is recalling Castile soap towelettes used in Foley trays and specimen kits because they are contaminated with bacteria.
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits because they are contaminated with bacteria.
FDA is recalling Castile soap towelettes in Foley trays and specimen kits due to bacterial contamination.
FDA is recalling specific lots of Castile soap towelettes used in medical kits because they are contaminated with bacteria.
The FDA is recalling Castile soap towelettes included in Foley trays and specimen kits because they are contaminated with bacteria.
The FDA is recalling Castile soap towelettes included in Foley trays and specimen kits due to bacterial contamination.
Castile soap towelettes used in Foley trays and specimen kits are recalled because they are contaminated with bacteria.
FDA is recalling Castile soap towelettes in Foley trays and specimen kits due to bacterial contamination.
FDA is recalling Aplicare Castile Soap towelettes found in medical kits due to bacterial contamination.
The FDA is recalling 1,010 units of pediatric feeding tubes because 8FR PVC tubes were incorrectly packaged in 6.5FR polyurethane packs.
The FDA is recalling 1,330 units of pediatric feeding tubes due to packaging errors where different tube sizes were placed in incorrect packages.
Covidien LLC is recalling 10 units of Palindrome Precision Chronic Catheter Kits due to incorrect packaging with a 90-degree bend at the distal tip.
Covidien LLC is recalling 365 units of Palindrome Precision Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.
Covidien LLC is recalling 280 units of Palindrome Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.
Covidien LLC is recalling 150 units of Palindrome Precision Chronic Catheter Kits due to incorrect packaging with a 90-degree bend at the distal tip.
Covidien LLC is recalling 160 units of Palindrome Precision Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
Covidien
Irish tax-registered company
Source: Wikidata (Q908172), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.