State
72,936 recalls have nationwide distribution and so reach Pennsylvania. 11,918 additional recalls listed Pennsylvania specifically in their distribution scope.
Of the 11,918 recalls naming Pennsylvania we have scored against our rubric, 1,922 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,866 (24%) are Severe.
Which agencies issued them
These figures cover only the 11,918 recalls whose distribution notice names Pennsylvania specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2025-2026 Chevrolet Express and GMC Savana cutaway vehicles because tires may have sidewall damage, increasing crash risk.
Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an electrical control unit error may prevent the vehicle from moving, increasing crash risk.
Cubimana Island Storm 3 In 1 Building Sets are being recalled because the battery compartment in the LED light piece lets children access button cell batteries.
HALO Magic Sleepsuits in three batch codes are being recalled because the zipper head can detach from the garment, posing a choking hazard to infants.
Prime Food Processing is recalling Dried Croaker Fish, 8 oz, because the fish is uneviscerated. The FDA has classified this recall as Class I, its most serious category.
Encore Medical, LP is recalling 14 EMPOWR 3D KNEE implants because they contain incorrect labeling. The recall affects US nationwide distribution.
Encore Medical, LP is recalling 20 Reverse Shoulder Prosthesis implants due to incorrect labeling. The recall affects nationwide distribution across multiple US states.
Wizcure Pharmaa is recalling all lots of Fluorescein Sodium Ophthalmic Strips because the products may not have been manufactured according to current good manufacturing practices, raising concerns about sterility assurance.
Agebox is recalling 665 bottles of iKids-Growth Day Formula capsules because they contain undeclared ibutamoren, a drug ingredient not approved for marketing in the U.S.
Olympus is recalling all lots of its Inner Sheath 21 Fr. Model A2660T used in urological procedures due to reports of the ceramic tip breaking during use.
Remel, Inc is recalling 97 units of Campy CVA Medium 100/PK, lot R01272, due to customer complaints reporting low to no recovery of Campylobacter Jejuni ATCC 33291. The product was distributed nationwide in AZ, CO, IL, NJ, OH, TN, and WA.
Medline is recalling 8,773 NAIL KIT (Model DYKM1528) units because the sterile saline wound wash may not have been manufactured to the required sterility assurance level for sterile products.
Medline Industries is recalling dialysis dressing change kits containing Tego Connectors due to potential silicone seal doming or tearing that may block fluid flow during use.
Olympus is recalling 207 units of its Resection Sheath, Model A22043T, after receiving complaints that the ceramic tip can break during use. The recall affects all lots distributed nationwide.
Olympus is recalling all lots of its Inner Sheath, Model A2641, used in urological endoscopic procedures, due to complaints that the ceramic tip can break during use.
Medline is recalling seven convenience kits used for dialysis maintenance because the silicone seal on the Tego Connectors may dome or tear, which can occlude the fluid path.
Olympus is recalling its Resection Sheath model A2666T, used for endoscopic diagnosis and treatment in urological applications, after complaints that the ceramic tip of the sheath can break.
SB Food LLC is recalling Yoyo Gummy Grape Plus Flavor, 2.8 oz bags, because the products contain an unallowed color, Carmoisine (E122) - Acid Red 14.
LEO Pharma is recalling its ADBRY injection drug due to particulate matter (wool fiber) found in one unit, which may affect sterility. The recall covers 11,407 units distributed nationwide.
Agebox is recalling iKids-Growth (Night Formula) 60-count bottles because the product was marketed without an approved NDA or ANDA and contains undeclared ibutamoren.
Medline is recalling five Trunk Kit convenience kits because the manufacturer of the sterile saline wound wash they contain may not have met the required sterility assurance level.
Navitas Organics is recalling organic chia seeds due to potential Salmonella contamination. The recall affects 114,432 units distributed across 26 U.S. states.
Gerber is recalling Arrowroot Biscuits in a downstream recall because they contain an arrowroot flour ingredient recalled by the supplier over potential contamination with soft kraft paper and plastic bag pieces.
Medline is recalling Nail Kit convenience kits, model POD14214, because the manufacturer of the sterile saline wound wash they contain may not have met the required sterility assurance level.
Olympus recalls 91 units of its Inner Sheath Model A4741 medical device after receiving complaints of the ceramic tip breaking during gynecological endoscopic procedures.