State
73,388 recalls have nationwide distribution and so reach Connecticut. 6,572 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,572 recalls naming Connecticut we have scored against our rubric, 838 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,881 (29%) are Severe.
Which agencies issued them
These figures cover only the 6,572 recalls whose distribution notice names Connecticut specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Abbott Laboratories is recalling Similac Special Care 2 fl oz bottles due to compromised seal integrity that could lead to spoilage. Affected bottles have batch number 41861N200 with a best-by date of 06/01/23.
The Bentex Group is recalling about 87,000 children's clothing sets because the textile ink contains lead levels that violate federal regulations. Lead is toxic if ingested and can cause health problems in young children.
Covidien recalls Endo Stitch V-Loc 180 automated suturing devices due to 210 reports of needles breaking during endoscopic surgery. Broken needle fragments may remain in patients, potentially causing tissue injury and requiring additional imaging.
Indigo Books & Music is recalling Papa Bear and Mama Bear ceramic mugs that can crack or break when filled with hot liquid, posing burn and laceration hazards. About 270 units were sold in the U.S.
Navistar is recalling 196 model-year 2023 IC BUS CESB buses due to defective fuel vapor lines. Without proper heat shielding, the lines may leak when exposed to exhaust heat, posing a fire risk.
Novapproach Spine is recalling OneLIF Torque Limiting Adapter components used in spinal surgery instruments because the adapter may not remain locked in the ratcheting handle once fully engaged. This could compromise surgical instrument function during use.
Abbott Laboratories recalls Pedialyte Unflavored 2 fl oz bottles for compromised seal integrity that could allow spoilage. Affected bottles were distributed across the United States and multiple countries.
Abbott Laboratories is recalling Similac 360 Total Care Sensitive infant formula in 2 fl oz bottles due to compromised seal integrity that could lead to spoilage. Approximately 15.9 million bottles are affected across the United States and international locations.
Steris recalls 5 GI4000 Electrosurgical Units with defective diode components that may cause power loss during endoscopic procedures.
Tollos is recalling Infection Control (IC) Lifting Straps used with certain Cirrus and Pinnacle ceiling lifts because the straps can break during patient lifts, potentially causing patients or caregivers to be injured by falls.
Altimate Medical is recalling EasyStand Bantam Small and Extra Small standers due to a component defect that may prevent the leg assembly bracket from maintaining the non-supine position. No injuries have been reported.
Abbott Laboratories is recalling batches of Similac 360 Total Care and Total Care Sensitive infant formula 2 fl oz discharge kits for compromised seal integrity that could allow spoilage. The affected batch is identified by product code 39480N200 with a Best By date of 04/01/23.
Sonendo Inc is recalling 15 GentleWave System APM Procedure Instruments (Model GW-APM-PI02) due to erroneous unit carton labels. The instruments were distributed worldwide, including Ohio and Canada.
Nephron Sterile Compounding Center is recalling 56,220 vials of PF-Neostigmine Methylsulfate Injection due to potential cross-contamination from manufacturing control deviations.
Abbott Laboratories is recalling specific lots of Similac Water due to compromised seal integrity that could lead to spoilage. The recall affects 14,588,544 bottles distributed across the US, territories, and international locations.
Sonendo Inc is recalling 16 GentleWave System Posterior CleanFlow procedure instruments with lot number W2022080204R due to erroneous unit carton labels that could affect proper identification and use.
Atrium Medical Corporation is recalling Atrium Ocean Wet Suction Water Seal Chest Drains (Product Code 2002-000) distributed in the United States due to warehouse temperature excursions in July and August 2021. No patient harm has been reported.
ATC is recalling 2022 Toyhauler-20-foot trailers because a welded seam on the electric retractable awning may separate, allowing the awning to drop and increase injury risk.
Volkswagen Group is recalling 2019-2022 Audi sedans, wagons, and allroad models. Liquid in the rear seat may penetrate and shut down the gateway control module, suddenly reducing engine power and increasing crash risk.
BMW is recalling 2023 740i, 760i, and i7 vehicles because the telematics unit may fail to send location data to emergency responders, potentially delaying aid.
Winnebago is recalling certain 2021-2023 Revel motorhomes because the retractable awning may extend unintentionally during transit, potentially becoming a distraction or road hazard.
Genuine Scooters is recalling 2022 Buddy Kick 125 motorcycles because a fuel pump defect may cause loss of drive power, increasing crash risk.
Coach and Equipment is recalling 2016-2023 Phoenix transit buses because zinc plating on fuel return lines may corrode, potentially causing fuel leaks and fire.
Shyft Group is recalling 2023 Utilimaster Walk-In vans because a retaining nut may loosen, allowing the bumper to detach and creating a road hazard.
E-One is recalling 2019-2021 Cyclone II and 2020-2021 Typhoon N emergency vehicles because exhaust heat buildup may cause a fire.