Pennsylvania recalls
3,667 federal recalls affecting Pennsylvania in the last 12 months - 307 Pennsylvania-specific plus 3,360 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-22FDA-DeviceArgon Medical DevicesClass INationwideArgon Medical pacing electrode trays recalled for sterility risk
Argon Medical Devices is recalling certain transvenous pacing electrode trays (model 008416A and 008566A) because they contain lidocaine ampules that did not meet sterility standards. The affected kits were distributed nationwide and internationally. No injuries have been reported.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Intro Kit introducer recalled for leakage risk
Abiomed heart pump introducer sheaths in the Intro Kit may leak fluid from under the sheath cap or along the hub score lines. The manufacturing defect is not visible to users. All current batches of the kit worldwide are affected.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP heart pump recalled for leakage risk
Abiomed has recalled the Impella CP heart pump due to a potential for fluid leakage from the introducer sheath (a tube inserted during the procedure). The leakage can occur under the sheath cap or along connection points, and these defects cannot be seen by the user. All current batches of the pump set are affected worldwide.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP heart pump recalled for sheath leakage risk
Abiomed has recalled its Impella CP Smart Assist Set heart pump due to a potential leak in the introducer sheath (a thin tube used during insertion). The leak can occur under the sheath cap or along seam lines in certain models, but the defect is not visible to the user. All current batches worldwide are affected.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP heart pump recalled for sheath leakage risk
Abiomed has recalled the Impella CP heart pump set due to a manufacturing defect in the introducer sheath that can cause leakage. The leakage can occur under the sheath cap or along hub score lines in the 14Fr and 23Fr introducers included with every pump set, and the defect is not visible to users.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella 5.5 heart pump recalled for sheath leakage risk
Abiomed has recalled certain Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a manufacturing defect in the introducer sheaths. The 14Fr and 23Fr introducers included in these pump sets may leak fluid from under the sheath cap or along hub seams, and the leakage cannot be seen by the user before or during use.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella 5.5 heart pump recalled for leakage risk
The Abiomed Impella 5.5 Smart Assist Set heart pump contains an introducer sheath that may leak under the cap or along hub seams. This manufacturing defect is not visible to the user but is present in all affected pump sets. The issue affects 383 units distributed worldwide.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Introducer Kit recalled for sheath leakage risk
Abiomed has recalled certain Introducer Kit 23 Fr units (Pump Set Code 1000441) due to a potential for sheath leakage from under the sheath cap and along hub score lines. This manufacturing issue cannot be seen by the user and affects introducers included in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP Introducer Kit recalled for leakage risk
Abiomed has recalled the Impella CP Introducer Kit (Pump Set Code 1000550) worldwide due to a potential for fluid leakage from under the sheath cap and along hub score lines in the 14Fr and 23Fr introducers. The leakage defect is not visible to the user and affects all current batches of this heart pump accessory kit.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP introducer recalled for leakage risk
Abiomed has recalled the Impella CP heart pump introducer due to a manufacturing defect that can cause fluid leakage from under the sheath cap and along the hub. The defect is not visible to the user and affects all current batches worldwide.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella RP Flex recalled for sheath leakage risk
The Abiomed Impella RP Flex heart pump set includes introducers that may leak fluid from under the sheath cap or along hub score lines due to manufacturing defects. These leaks cannot be seen by visual inspection. All current batches worldwide are affected.
- 2026-07-22FDA-FoodGellert GlobalClass IIGellert Global Group artichoke hearts recalled for glass
Glass fragments were found in Gellert Global Group Ruby brand artichoke hearts (5 lb 8 oz cans). The affected product was distributed to New York, Pennsylvania, New Jersey, and Connecticut. About 1,150 cases are involved.
- 2026-07-22FDA-FoodAmy's KitchenClass IIAmy's Kitchen lentil soup recalled for spoilage risk
Amy's Kitchen organic lentil soup (light in sodium, 14.5 oz cans) with lot code 60D0924 and best-before date of April 2027 may spoil before the printed date. The affected product was distributed across the U.S. and Canada.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Nanche ice pops recalled for undeclared allergens
D'Dioses Fruit Pops, Inc. is recalling Nanche ice pops that may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. These allergens are not listed on the package label. The affected product was distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Tamarindo ice pops recalled for undeclared allergens
D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. These allergens are not listed on the package label. The affected product is the Tamarindo flavor in 1-bar (81.7 g) packages, distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Mango ice pops recalled for undeclared allergens
D'Dioses Mango ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. These allergens are not listed on the package label. The recall affects 167 cases distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Grocella ice pops recalled for undeclared allergens
D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. People with allergies or sensitivities to these ingredients could have a serious reaction if they consume the product without knowing these allergens are present.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Limon ice pops recalled for undeclared allergens
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Limon 4 oz ice pops because they may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40 dye. The affected products were distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Pina Colada ice pop recalled for undeclared allergens
D'Dioses Fruit Pops, Inc. is recalling Pina Colada ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in New Jersey, Connecticut, New York, and Pennsylvania. People with allergies or sensitivities to these ingredients could have a serious reaction if they consume the product.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Cookies Cream ice pop recalled for undeclared allergens
D'Dioses Fruit Pops, Inc. is recalling Cookies Cream ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. These allergens are not listed on the package label and could pose a serious risk to people with allergies or sensitivities to these ingredients.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Nuez ice pops recalled for undeclared allergens
D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. The product was distributed in New Jersey, Connecticut, New York, and Pennsylvania. People with allergies or sensitivities to these ingredients could have a serious reaction if they consume the product without knowing about these allergens.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Pistachio ice pop recalled for undeclared allergens
D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. These allergens are not listed on the package label. People with allergies or sensitivities to these ingredients could have a serious reaction.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Rompope ice pops recalled for undeclared allergens
D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40 dyes. These allergens are not listed on the label and could pose a serious risk to people with allergies or sensitivities. The product was distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Vainilla ice pops recalled for undeclared allergens
D'Dioses Vainilla ice pops (4 oz) may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. These allergens are not listed on the package label. The affected ice pops were distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Guayaba ice pops recalled for undeclared allergens
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Guayaba ice pops because they may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. These allergens are not listed on the label and could cause serious reactions in people with allergies or sensitivities.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Mamey ice pops recalled for undeclared allergens
D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in New Jersey, Connecticut, New York, and Pennsylvania. People with allergies or sensitivities to these ingredients could have a serious reaction if they consume the product without knowing these allergens are present.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses ice pops recalled for undeclared milk, nuts, dyes
D'Dioses Arroz con Leche ice pops (4 oz) may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. These allergens and dyes are not listed on the label. The affected product was distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Fresa Leche ice pops recalled for undeclared allergens
D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. These allergens are not listed on the label and can cause serious reactions in people with allergies or sensitivities. The affected products were distributed in New Jersey, Connecticut, New York, and Pennsylvania.
- 2026-07-22FDA-FoodD'Dioses Fruit PopsClass ID'Dioses Coconut Ice Pops recalled for undeclared allergens
D'Dioses Coconut Ice Pops (4 oz) may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. These allergens are not listed on the package label. People with allergies or sensitivities to milk, tree nuts, or these food dyes could have a serious reaction.
- 2026-07-22FDA-FoodW.Y. IndustriesClass IIW.Y. Industries duck sauce recalled for metal fragments
W.Y. Industries is recalling duck sauce packets after discovering they may contain metal fragments. The affected packets are 0.35 oz. flexible film packets sold in cases of 500. The issue affects specific lot codes and was distributed to New York, New Jersey, Ohio, and Pennsylvania.
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