[pending] 2023 PETERBILT 548
Pending LLM rewrite. Source: NHTSA 25V014000.
- Product
- PETERBILT — 2023 PETERBILT 548
- Category
- Vehicle
- Distribution
- Distributed nationwide
State
19,713 recalls have nationwide distribution and so reach Iowa. 0 additional recalls listed Iowa specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Iowa consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Pending LLM rewrite. Source: NHTSA 25V014000.
Pending LLM rewrite. Source: FDA_DRUG D-0401-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1604-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1610-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1600-2026.
Western Mixers Produce & Nuts, Inc. is recalling First Street Chilli Spanish Peanuts (11 oz) because glass fragments were found in sealed containers. Affected lots have expiration dates of 2/11/2027, 2/13/2027, and 2/23/2027.
Pending LLM rewrite. Source: FDA_DEVICE Z-1650-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1641-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1616-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1624-2026.
Pending LLM rewrite. Source: NHTSA 25V018000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1598-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1568-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1611-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1620-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1632-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1639-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0406-2026.
Pending LLM rewrite. Source: NHTSA 25V015000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1603-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1617-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1590-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1625-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1635-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1631-2026.